메뉴 건너뛰기




Volumn 45, Issue 18, 2009, Pages 3228-3236

Variants of the xeroderma pigmentosum variant gene (POLH) are associated with melanoma risk

Author keywords

DNA repair; Melanoma genetics; POLH; Polymorphism; Xeroderma pigmentosum

Indexed keywords

DNA POLYMERASE;

EID: 70450231742     PISSN: 09598049     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejca.2009.04.034     Document Type: Article
Times cited : (35)

References (49)
  • 1
    • 0041412922 scopus 로고    scopus 로고
    • Changing epidemiology of malignant cutaneous melanoma in Europe 1953-1997: rising trends in incidence and mortality but recent stabilizations in western Europe and decreases in Scandinavia
    • de Vries E., Bray F.I., Coebergh J.W., and Parkin D.M. Changing epidemiology of malignant cutaneous melanoma in Europe 1953-1997: rising trends in incidence and mortality but recent stabilizations in western Europe and decreases in Scandinavia. Int J Cancer 107 1 (2003) 119-126
    • (2003) Int J Cancer , vol.107 , Issue.1 , pp. 119-126
    • de Vries, E.1    Bray, F.I.2    Coebergh, J.W.3    Parkin, D.M.4
  • 2
    • 0347356319 scopus 로고    scopus 로고
    • Epidemiology of cutaneous melanoma and non-melanoma skin cancer in Schleswig-Holstein, Germany: incidence, clinical subtypes, tumour stages and localization (epidemiology of skin cancer)
    • Katalinic A., Kunze U., and Schafer T. Epidemiology of cutaneous melanoma and non-melanoma skin cancer in Schleswig-Holstein, Germany: incidence, clinical subtypes, tumour stages and localization (epidemiology of skin cancer). Brit J Dermatol 149 6 (2003) 1200-1206
    • (2003) Brit J Dermatol , vol.149 , Issue.6 , pp. 1200-1206
    • Katalinic, A.1    Kunze, U.2    Schafer, T.3
  • 3
    • 55949120590 scopus 로고    scopus 로고
    • Distribution of melanoma incidence and mortality by age, 2001-2005
    • StatBite: Distribution of melanoma incidence and mortality by age, 2001-2005. J Natl Cancer Inst 2008;100(21):1498.
    • (2008) J Natl Cancer Inst , vol.100 , Issue.21 , pp. 1498
    • StatBite1
  • 5
    • 0028121279 scopus 로고
    • A cell cycle regulator potentially involved in genesis of many tumor types
    • Kamb A., Gruis N.A., Weaver-Feldhaus J., Liu Q., Harshman K., Tavtigian S.V., et al. A cell cycle regulator potentially involved in genesis of many tumor types. Science 264 5157 (1994) 436-440
    • (1994) Science , vol.264 , Issue.5157 , pp. 436-440
    • Kamb, A.1    Gruis, N.A.2    Weaver-Feldhaus, J.3    Liu, Q.4    Harshman, K.5    Tavtigian, S.V.6
  • 6
    • 0029664339 scopus 로고    scopus 로고
    • Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
    • Zuo L., Weger J., Yang Q., Goldstein A.M., Tucker M.A., Walker G.J., et al. Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma. Nat Genet 12 1 (1996) 97-99
    • (1996) Nat Genet , vol.12 , Issue.1 , pp. 97-99
    • Zuo, L.1    Weger, J.2    Yang, Q.3    Goldstein, A.M.4    Tucker, M.A.5    Walker, G.J.6
  • 9
    • 51549103690 scopus 로고    scopus 로고
    • Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population
    • Guedj M., Bourillon A., Combadieres C., Rodero M., Dieude P., Descamps V., et al. Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population. Human Mutat 29 9 (2008) 1154-1160
    • (2008) Human Mutat , vol.29 , Issue.9 , pp. 1154-1160
    • Guedj, M.1    Bourillon, A.2    Combadieres, C.3    Rodero, M.4    Dieude, P.5    Descamps, V.6
  • 10
    • 0033910271 scopus 로고    scopus 로고
    • Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?
    • Palmer J.S., Duffy D.L., Box N.F., Aitken J.F., O'Gorman L.E., Green A.C., et al. Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?. Am J Human Genet 66 1 (2000) 176-186
    • (2000) Am J Human Genet , vol.66 , Issue.1 , pp. 176-186
    • Palmer, J.S.1    Duffy, D.L.2    Box, N.F.3    Aitken, J.F.4    O'Gorman, L.E.5    Green, A.C.6
  • 11
    • 45549097424 scopus 로고    scopus 로고
    • ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
    • Gudbjartsson D.F., Sulem P., Stacey S.N., Goldstein A.M., Rafnar T., Sigurgeirsson B., et al. ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. Nat Genet 40 7 (2008) 886-891
    • (2008) Nat Genet , vol.40 , Issue.7 , pp. 886-891
    • Gudbjartsson, D.F.1    Sulem, P.2    Stacey, S.N.3    Goldstein, A.M.4    Rafnar, T.5    Sigurgeirsson, B.6
  • 12
    • 0037902558 scopus 로고    scopus 로고
    • The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes
    • Sturm R.A., Duffy D.L., Box N.F., Chen W., Smit D.J., Brown D.L., et al. The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes. Pigment Cell Res 16 3 (2003) 266-272
    • (2003) Pigment Cell Res , vol.16 , Issue.3 , pp. 266-272
    • Sturm, R.A.1    Duffy, D.L.2    Box, N.F.3    Chen, W.4    Smit, D.J.5    Brown, D.L.6
  • 14
    • 14944367557 scopus 로고    scopus 로고
    • Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation
    • Graf J., Hodgson R., and van Daal A. Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation. Human Mutat 25 3 (2005) 278-284
    • (2005) Human Mutat , vol.25 , Issue.3 , pp. 278-284
    • Graf, J.1    Hodgson, R.2    van Daal, A.3
  • 18
    • 0036256959 scopus 로고    scopus 로고
    • The genetics of the hereditary xeroderma pigmentosum syndrome
    • Stary A., and Sarasin A. The genetics of the hereditary xeroderma pigmentosum syndrome. Biochimie 84 1 (2002) 49-60
    • (2002) Biochimie , vol.84 , Issue.1 , pp. 49-60
    • Stary, A.1    Sarasin, A.2
  • 20
    • 0034667360 scopus 로고    scopus 로고
    • A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer
    • Winsey S.L., Haldar N.A., Marsh H.P., Bunce M., Marshall S.E., Harris A.L., et al. A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer. Cancer Res 60 20 (2000) 5612-5616
    • (2000) Cancer Res , vol.60 , Issue.20 , pp. 5612-5616
    • Winsey, S.L.1    Haldar, N.A.2    Marsh, H.P.3    Bunce, M.4    Marshall, S.E.5    Harris, A.L.6
  • 21
    • 34447099199 scopus 로고    scopus 로고
    • DNA repair gene polymorphisms and genetic predisposition to cutaneous melanoma
    • Povey J.E., Darakhshan F., Robertson K., Bisset Y., Mekky M., Rees J., et al. DNA repair gene polymorphisms and genetic predisposition to cutaneous melanoma. Carcinogenesis 28 5 (2007) 1087-1093
    • (2007) Carcinogenesis , vol.28 , Issue.5 , pp. 1087-1093
    • Povey, J.E.1    Darakhshan, F.2    Robertson, K.3    Bisset, Y.4    Mekky, M.5    Rees, J.6
  • 22
    • 10744233034 scopus 로고    scopus 로고
    • XPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma risk
    • Baccarelli A., Calista D., Minghetti P., Marinelli B., Albetti B., Tseng T., et al. XPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma risk. Brit J Cancer 90 2 (2004) 497-502
    • (2004) Brit J Cancer , vol.90 , Issue.2 , pp. 497-502
    • Baccarelli, A.1    Calista, D.2    Minghetti, P.3    Marinelli, B.4    Albetti, B.5    Tseng, T.6
  • 23
    • 13544253717 scopus 로고    scopus 로고
    • No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanoma
    • Blankenburg S., Konig I.R., Moessner R., Laspe P., Thoms K.M., Krueger U., et al. No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanoma. Eur J Human Genet 13 2 (2005) 253-255
    • (2005) Eur J Human Genet , vol.13 , Issue.2 , pp. 253-255
    • Blankenburg, S.1    Konig, I.R.2    Moessner, R.3    Laspe, P.4    Thoms, K.M.5    Krueger, U.6
  • 25
    • 49849097913 scopus 로고    scopus 로고
    • The Gln/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys/Gln as an important predictor for melanoma progression: a case control study in the Swedish population
    • Kertat K., Rosdahl I., Sun X.F., Synnerstad I., and Zhang H. The Gln/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys/Gln as an important predictor for melanoma progression: a case control study in the Swedish population. Oncol Rep 20 1 (2008) 179-183
    • (2008) Oncol Rep , vol.20 , Issue.1 , pp. 179-183
    • Kertat, K.1    Rosdahl, I.2    Sun, X.F.3    Synnerstad, I.4    Zhang, H.5
  • 26
    • 0036802254 scopus 로고    scopus 로고
    • DNA repair gene XRCC3 241Met variant is not associated with risk of cutaneous malignant melanoma
    • Duan Z., Shen H., Lee J.E., Gershenwald J.E., Ross M.I., Mansfield P.F., et al. DNA repair gene XRCC3 241Met variant is not associated with risk of cutaneous malignant melanoma. Cancer Epidemiol Biomark Prev 11 10 Pt 1 (2002) 1142-1143
    • (2002) Cancer Epidemiol Biomark Prev , vol.11 , Issue.10 PART 1 , pp. 1142-1143
    • Duan, Z.1    Shen, H.2    Lee, J.E.3    Gershenwald, J.E.4    Ross, M.I.5    Mansfield, P.F.6
  • 27
    • 2342512130 scopus 로고    scopus 로고
    • Polymorphisms in DNA double-strand break repair genes and skin cancer risk
    • Han J., Colditz G.A., Samson L.D., and Hunter D.J. Polymorphisms in DNA double-strand break repair genes and skin cancer risk. Cancer Res 64 9 (2004) 3009-3013
    • (2004) Cancer Res , vol.64 , Issue.9 , pp. 3009-3013
    • Han, J.1    Colditz, G.A.2    Samson, L.D.3    Hunter, D.J.4
  • 28
    • 20444400600 scopus 로고    scopus 로고
    • Genetic variation in XPD, sun exposure, and risk of skin cancer
    • Han J., Colditz G.A., Liu J.S., and Hunter D.J. Genetic variation in XPD, sun exposure, and risk of skin cancer. Cancer Epidemiol Biomark Prev 14 6 (2005) 1539-1544
    • (2005) Cancer Epidemiol Biomark Prev , vol.14 , Issue.6 , pp. 1539-1544
    • Han, J.1    Colditz, G.A.2    Liu, J.S.3    Hunter, D.J.4
  • 29
    • 33845988014 scopus 로고    scopus 로고
    • Polymorphisms in the DNA repair genes XPC, XPD, and XPG and risk of cutaneous melanoma: a case-control analysis
    • Li C., Hu Z., Liu Z., Wang L.E., Strom S.S., Gershenwald J.E., et al. Polymorphisms in the DNA repair genes XPC, XPD, and XPG and risk of cutaneous melanoma: a case-control analysis. Cancer Epidemiol Biomark Prev 15 12 (2006) 2526-2532
    • (2006) Cancer Epidemiol Biomark Prev , vol.15 , Issue.12 , pp. 2526-2532
    • Li, C.1    Hu, Z.2    Liu, Z.3    Wang, L.E.4    Strom, S.S.5    Gershenwald, J.E.6
  • 30
    • 0035093514 scopus 로고    scopus 로고
    • Nucleotide excision repair gene XPD polymorphisms and genetic predisposition to melanoma
    • Tomescu D., Kavanagh G., Ha T., Campbell H., and Melton D.W. Nucleotide excision repair gene XPD polymorphisms and genetic predisposition to melanoma. Carcinogenesis 22 3 (2001) 403-408
    • (2001) Carcinogenesis , vol.22 , Issue.3 , pp. 403-408
    • Tomescu, D.1    Kavanagh, G.2    Ha, T.3    Campbell, H.4    Melton, D.W.5
  • 31
    • 22344450281 scopus 로고    scopus 로고
    • Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study
    • Blankenburg S., Konig I.R., Moessner R., Laspe P., Thoms K.M., Krueger U., et al. Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study. Carcinogenesis 26 6 (2005) 1085-1090
    • (2005) Carcinogenesis , vol.26 , Issue.6 , pp. 1085-1090
    • Blankenburg, S.1    Konig, I.R.2    Moessner, R.3    Laspe, P.4    Thoms, K.M.5    Krueger, U.6
  • 32
    • 0033578040 scopus 로고    scopus 로고
    • The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta
    • Masutani C., Kusumoto R., Yamada A., Dohmae N., Yokoi M., Yuasa M., et al. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta. Nature 399 6737 (1999) 700-704
    • (1999) Nature , vol.399 , Issue.6737 , pp. 700-704
    • Masutani, C.1    Kusumoto, R.2    Yamada, A.3    Dohmae, N.4    Yokoi, M.5    Yuasa, M.6
  • 33
    • 0034521292 scopus 로고    scopus 로고
    • Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiation
    • Itoh T., Linn S., Kamide R., Tokushige H., Katori N., Hosaka Y., et al. Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiation. J Invest Dermatol 115 6 (2000) 981-985
    • (2000) J Invest Dermatol , vol.115 , Issue.6 , pp. 981-985
    • Itoh, T.1    Linn, S.2    Kamide, R.3    Tokushige, H.4    Katori, N.5    Hosaka, Y.6
  • 34
    • 0033538470 scopus 로고    scopus 로고
    • HRAD30 mutations in the variant form of xeroderma pigmentosum
    • Johnson R.E., Kondratick C.M., Prakash S., and Prakash L. HRAD30 mutations in the variant form of xeroderma pigmentosum. Science 285 5425 (1999) 263-265
    • (1999) Science , vol.285 , Issue.5425 , pp. 263-265
    • Johnson, R.E.1    Kondratick, C.M.2    Prakash, S.3    Prakash, L.4
  • 35
    • 0034726962 scopus 로고    scopus 로고
    • Genomic structure, chromosomal localization and identification of mutations in the xeroderma pigmentosum variant (XPV) gene
    • Yuasa M., Masutani C., Eki T., and Hanaoka F. Genomic structure, chromosomal localization and identification of mutations in the xeroderma pigmentosum variant (XPV) gene. Oncogene 19 41 (2000) 4721-4728
    • (2000) Oncogene , vol.19 , Issue.41 , pp. 4721-4728
    • Yuasa, M.1    Masutani, C.2    Eki, T.3    Hanaoka, F.4
  • 37
    • 0142025110 scopus 로고    scopus 로고
    • Molecular genetics of xeroderma pigmentosum variant
    • Gratchev A., Strein P., Utikal J., and Sergij G. Molecular genetics of xeroderma pigmentosum variant. Exp Dermatol 12 5 (2003) 529-536
    • (2003) Exp Dermatol , vol.12 , Issue.5 , pp. 529-536
    • Gratchev, A.1    Strein, P.2    Utikal, J.3    Sergij, G.4
  • 38
    • 34250690390 scopus 로고    scopus 로고
    • Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as xeroderma pigmentosum variant type
    • Tanioka M., Masaki T., Ono R., Nagano T., Otoshi-Honda E., Matsumura Y., et al. Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as xeroderma pigmentosum variant type. J Invest Dermatol 127 7 (2007) 1745-1751
    • (2007) J Invest Dermatol , vol.127 , Issue.7 , pp. 1745-1751
    • Tanioka, M.1    Masaki, T.2    Ono, R.3    Nagano, T.4    Otoshi-Honda, E.5    Matsumura, Y.6
  • 39
    • 47349099501 scopus 로고    scopus 로고
    • Xeroderma pigmentosum-variant patients from America, Europe, and Asia
    • Inui H., Oh K.S., Nadem C., Ueda T., Khan S.G., Metin A., et al. Xeroderma pigmentosum-variant patients from America, Europe, and Asia. J Invest Dermatol 128 8 (2008) 2055-2068
    • (2008) J Invest Dermatol , vol.128 , Issue.8 , pp. 2055-2068
    • Inui, H.1    Oh, K.S.2    Nadem, C.3    Ueda, T.4    Khan, S.G.5    Metin, A.6
  • 40
    • 0033983935 scopus 로고    scopus 로고
    • Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum
    • Cleaver J.E. Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum. J Dermatol Sci 23 1 (2000) 1-11
    • (2000) J Dermatol Sci , vol.23 , Issue.1 , pp. 1-11
    • Cleaver, J.E.1
  • 41
    • 0035862988 scopus 로고    scopus 로고
    • Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells
    • Kannouche P., Broughton B.C., Volker M., Hanaoka F., Mullenders L.H., and Lehmann A.R. Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells. Genes Dev 15 2 (2001) 158-172
    • (2001) Genes Dev , vol.15 , Issue.2 , pp. 158-172
    • Kannouche, P.1    Broughton, B.C.2    Volker, M.3    Hanaoka, F.4    Mullenders, L.H.5    Lehmann, A.R.6
  • 42
    • 33749602964 scopus 로고    scopus 로고
    • UV-B radiation induces epithelial tumors in mice lacking DNA polymerase eta and mesenchymal tumors in mice deficient for DNA polymerase iota
    • Ohkumo T., Kondo Y., Yokoi M., Tsukamoto T., Yamada A., Sugimoto T., et al. UV-B radiation induces epithelial tumors in mice lacking DNA polymerase eta and mesenchymal tumors in mice deficient for DNA polymerase iota. Mol Cell Biol 26 20 (2006) 7696-7706
    • (2006) Mol Cell Biol , vol.26 , Issue.20 , pp. 7696-7706
    • Ohkumo, T.1    Kondo, Y.2    Yokoi, M.3    Tsukamoto, T.4    Yamada, A.5    Sugimoto, T.6
  • 43
    • 45149121724 scopus 로고    scopus 로고
    • Testing for linkage and association with rheumatoid arthritis a ptpn22 promoter polymorphism reported to be associated and linked with type 1 diabetes in the Caucasian population
    • Dieude P., Teixeira V.H., Pierlot C., Cornelis F., and Petit-Teixeira E. Testing for linkage and association with rheumatoid arthritis a ptpn22 promoter polymorphism reported to be associated and linked with type 1 diabetes in the Caucasian population. Ann Rheum Dis 67 6 (2008) 900-901
    • (2008) Ann Rheum Dis , vol.67 , Issue.6 , pp. 900-901
    • Dieude, P.1    Teixeira, V.H.2    Pierlot, C.3    Cornelis, F.4    Petit-Teixeira, E.5
  • 44
    • 33847338933 scopus 로고    scopus 로고
    • Structure of the ubiquitin-binding zinc finger domain of human DNA Y-polymerase eta
    • Bomar M.G., Pai M.T., Tzeng S.R., Li S.S., and Zhou P. Structure of the ubiquitin-binding zinc finger domain of human DNA Y-polymerase eta. EMBO Rep 8 3 (2007) 247-251
    • (2007) EMBO Rep , vol.8 , Issue.3 , pp. 247-251
    • Bomar, M.G.1    Pai, M.T.2    Tzeng, S.R.3    Li, S.S.4    Zhou, P.5
  • 45
    • 36048931023 scopus 로고    scopus 로고
    • Bypass of DNA lesions generated during anticancer treatment with cisplatin by DNA polymerase eta
    • Alt A., Lammens K., Chiocchini C., Lammens A., Pieck J.C., Kuch D., et al. Bypass of DNA lesions generated during anticancer treatment with cisplatin by DNA polymerase eta. Science 318 5852 (2007) 967-970
    • (2007) Science , vol.318 , Issue.5852 , pp. 967-970
    • Alt, A.1    Lammens, K.2    Chiocchini, C.3    Lammens, A.4    Pieck, J.C.5    Kuch, D.6
  • 46
    • 0034847259 scopus 로고    scopus 로고
    • Structure of the catalytic core of S. cerevisiae DNA polymerase eta: implications for translesion DNA synthesis
    • Trincao J., Johnson R.E., Escalante C.R., Prakash S., Prakash L., Aggarwal A.K., et al. Structure of the catalytic core of S. cerevisiae DNA polymerase eta: implications for translesion DNA synthesis. Mol Cell 8 2 (2001) 417-426
    • (2001) Mol Cell , vol.8 , Issue.2 , pp. 417-426
    • Trincao, J.1    Johnson, R.E.2    Escalante, C.R.3    Prakash, S.4    Prakash, L.5    Aggarwal, A.K.6
  • 47
    • 47249105581 scopus 로고    scopus 로고
    • The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis
    • Dieude P., Guedj M., Wipff J., Avouac J., Hachulla E., Diot E., et al. The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis. Arthritis Rheum 58 7 (2008) 2183-2188
    • (2008) Arthritis Rheum , vol.58 , Issue.7 , pp. 2183-2188
    • Dieude, P.1    Guedj, M.2    Wipff, J.3    Avouac, J.4    Hachulla, E.5    Diot, E.6
  • 48
    • 31544443220 scopus 로고    scopus 로고
    • Increased susceptibility to UV-induced skin carcinogenesis in polymerase eta-deficient mice
    • Lin Q., Clark A.B., McCulloch S.D., Yuan T., Bronson R.T., Kunkel T.A., et al. Increased susceptibility to UV-induced skin carcinogenesis in polymerase eta-deficient mice. Cancer Res 66 1 (2006) 87-94
    • (2006) Cancer Res , vol.66 , Issue.1 , pp. 87-94
    • Lin, Q.1    Clark, A.B.2    McCulloch, S.D.3    Yuan, T.4    Bronson, R.T.5    Kunkel, T.A.6
  • 49
    • 0034837773 scopus 로고    scopus 로고
    • MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
    • Box N.F., Duffy D.L., Chen W., Stark M., Martin N.G., Sturm R.A., et al. MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. Am J Human Genet 69 4 (2001) 765-773
    • (2001) Am J Human Genet , vol.69 , Issue.4 , pp. 765-773
    • Box, N.F.1    Duffy, D.L.2    Chen, W.3    Stark, M.4    Martin, N.G.5    Sturm, R.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.