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Volumn 63, Issue 2, 2000, Pages 271-278

Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 11Q; DEMYELINATION; GENE MAPPING; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; PRIORITY JOURNAL;

EID: 0034051581     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.6088     Document Type: Article
Times cited : (20)

References (26)
  • 4
    • 0030015647 scopus 로고    scopus 로고
    • Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing
    • Bolino A., Brancolini V., Bono F., Bruni A., Gambardella A., Romeo G., Quattrone A., Devoto M. Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing. Hum. Mol. Genet. 5:1996;1051-1054.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1051-1054
    • Bolino, A.1    Brancolini, V.2    Bono, F.3    Bruni, A.4    Gambardella, A.5    Romeo, G.6    Quattrone, A.7    Devoto, M.8
  • 7
    • 0001046663 scopus 로고
    • Hereditary motor and sensory neuropathies
    • P. J. Dyck, P. K. Thomas, J. W. Griffin, P. A. Low, & J. F. Poduslo. Philadelphia: Saunders
    • Dyck P. J., Chance P., Lebo R., Carney J. A. Hereditary motor and sensory neuropathies. Dyck P. J., Thomas P. K., Griffin J. W., Low P. A., Poduslo J. F. Peripheral Neuropathy. 1993;1094-1136 Saunders, Philadelphia.
    • (1993) Peripheral Neuropathy , pp. 1094-1136
    • Dyck, P.J.1    Chance, P.2    Lebo, R.3    Carney, J.A.4
  • 9
    • 0030859638 scopus 로고    scopus 로고
    • Hereditary demyelinating neuropathy of infancy: A genetically complex syndrome
    • Gambardella A., Muglia M., Quattrone A. Hereditary demyelinating neuropathy of infancy: A genetically complex syndrome. Brain. 120:1997;2113-2115.
    • (1997) Brain , vol.120 , pp. 2113-2115
    • Gambardella, A.1    Muglia, M.2    Quattrone, A.3
  • 11
    • 0025016822 scopus 로고
    • Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction
    • Green E. D., Olson M. V. Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction. Proc. Natl. Acad. Sci. USA. 87:1990;1213-1217.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 1213-1217
    • Green, E.D.1    Olson, M.V.2
  • 13
    • 0029849358 scopus 로고    scopus 로고
    • Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33
    • LeGuern E., Guilbot A., Kessali M., Ravise N., Tassin J., Maisonobe T., Grid D., Brice A. Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. Hum. Mol. Genet. 5:1996;1685-1688.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1685-1688
    • Leguern, E.1    Guilbot, A.2    Kessali, M.3    Ravise, N.4    Tassin, J.5    Maisonobe, T.6    Grid, D.7    Brice, A.8
  • 15
    • 0030668164 scopus 로고    scopus 로고
    • Advances in Charcot-Marie-Tooth disease research: Cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms
    • Muller H. W., Suter U., Van Broeckhoven C. Advances in Charcot-Marie-Tooth disease research: Cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. Neurobiol. Dis. 4:1997;215-220.
    • (1997) Neurobiol. Dis. , vol.4 , pp. 215-220
    • Muller, H.W.1    Suter, U.2    Van Broeckhoven, C.3
  • 16
    • 0029186023 scopus 로고
    • Prediction of the coding sequences of unidentified human genes. III. The coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1
    • Nagase T., Miyajima N., Tanaka A., Sazuka T., Seki N., Sato S., Tabata S., Ishikawa K., Kawarabayasi Y., Kotani H. Prediction of the coding sequences of unidentified human genes. III. The coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1. DNA Res. 2:1995;51-59.
    • (1995) DNA Res. , vol.2 , pp. 51-59
    • Nagase, T.1    Miyajima, N.2    Tanaka, A.3    Sazuka, T.4    Seki, N.5    Sato, S.6    Tabata, S.7    Ishikawa, K.8    Kawarabayasi, Y.9    Kotani, H.10
  • 17
    • 0032585352 scopus 로고    scopus 로고
    • Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
    • Nagase T., Ishikawa K., Suyama M., Kikuno R., Hirosawa M., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O. Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. DNA Res. 5:1998;355-364.
    • (1998) DNA Res. , vol.5 , pp. 355-364
    • Nagase, T.1    Ishikawa, K.2    Suyama, M.3    Kikuno, R.4    Hirosawa, M.5    Miyajima, N.6    Tanaka, A.7    Kotani, H.8    Nomura, N.9    Ohara, O.10
  • 19
    • 0032948117 scopus 로고    scopus 로고
    • Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies
    • Nelis E., Haites N., Van Broeckhoven C. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. Hum. Mutat. 13:1999;11-28.
    • (1999) Hum. Mutat. , vol.13 , pp. 11-28
    • Nelis, E.1    Haites, N.2    Van Broeckhoven, C.3
  • 25
    • 0031943222 scopus 로고    scopus 로고
    • Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
    • Warner L. E., Mancias P., Butler I. J., McDonald C. M., Keppen L., Koob K. G., Lupski J. R. Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies. Nat. Genet. 18:1998;382-384.
    • (1998) Nat. Genet. , vol.18 , pp. 382-384
    • Warner, L.E.1    Mancias, P.2    Butler, I.J.3    McDonald, C.M.4    Keppen, L.5    Koob, K.G.6    Lupski, J.R.7
  • 26
    • 0024582686 scopus 로고
    • Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
    • Weber J. L., May P. E. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet. 44:1989;388-396.
    • (1989) Am. J. Hum. Genet. , vol.44 , pp. 388-396
    • Weber, J.L.1    May, P.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.