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Volumn 21, Issue 6, 2003, Pages 577-581

Human Gene Mutation Database (HGMD®): 2003 Update

Author keywords

Bioinformatics; HGMD; Human; Inherited disease; Mutation database

Indexed keywords

COMPLEMENTARY DNA;

EID: 0037903275     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10212     Document Type: Review
Times cited : (1555)

References (17)
  • 2
    • 0036107052 scopus 로고    scopus 로고
    • Time for a unified system of mutation description and reporting: A review of locus-specific mutation databases
    • Claustres M, Horaitis O, Vanevski M, Cotton RGH. 2002. Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases. Genome Res 12:680-688.
    • (2002) Genome Res , vol.12 , pp. 680-688
    • Claustres, M.1    Horaitis, O.2    Vanevski, M.3    Cotton, R.G.H.4
  • 4
    • 0036523997 scopus 로고    scopus 로고
    • Proposed guidelines for papers describing DNA polymorphism- disease associations
    • Cooper DN, Nussbaum RL, Krawczak M. 2002. Proposed guidelines for papers describing DNA polymorphism- disease associations. Hum Genet 110:207-208.
    • (2002) Hum Genet , vol.110 , pp. 207-208
    • Cooper, D.N.1    Nussbaum, R.L.2    Krawczak, M.3
  • 5
    • 0033986101 scopus 로고    scopus 로고
    • Future vision of the GDB human genome database
    • Cuticchia AJ. 2000. Future vision of the GDB human genome database. Hum Mutat 15:62-67.
    • (2000) Hum Mutat , vol.15 , pp. 62-67
    • Cuticchia, A.J.1
  • 6
    • 0034908554 scopus 로고    scopus 로고
    • Nomenclature recommendations: Nomenclature for the description of human sequence variations
    • den Dunnen JT, Antonarakis SE 2001. Nomenclature recommendations: nomenclature for the description of human sequence variations. Hum Genet 109:121-124.
    • (2001) Hum Genet , vol.109 , pp. 121-124
    • Den Dunnen, J.T.1    Antonarakis, S.E.2
  • 7
    • 0036081484 scopus 로고    scopus 로고
    • HGVbase: A human sequence variation database emphasizing data quality and a broad spectrum of data sources
    • Fredman D, Siegfried M, Yuan YP, Bork P, Lehvaslaiho H, Brookes AJ. 2002. HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources. Nucleic Acids Res 30:387-391.
    • (2002) Nucleic Acids Res , vol.30 , pp. 387-391
    • Fredman, D.1    Siegfried, M.2    Yuan, Y.P.3    Bork, P.4    Lehvaslaiho, H.5    Brookes, A.J.6
  • 8
    • 0345363156 scopus 로고    scopus 로고
    • Genatlas database, genes and development defects
    • Frézal J. 1998. Genatlas database, genes and development defects. C R Acad Sci III 321:805-817.
    • (1998) C R Acad Sci III , vol.321 , pp. 805-817
    • Frézal, J.1
  • 9
  • 12
    • 0031092272 scopus 로고    scopus 로고
    • The human gene mutation database
    • Krawczak M, Cooper DN. 1997. The Human Gene Mutation Database. Trends Genet 13:121-122.
    • (1997) Trends Genet , vol.13 , pp. 121-122
    • Krawczak, M.1    Cooper, D.N.2
  • 16
    • 0035162594 scopus 로고    scopus 로고
    • RefSeq and LocusLink: NCBI gene-centered resources
    • Pruitt KD, Maglott DR. 2001. RefSeq and LocusLink: NCBI gene-centered resources. Nucleic Acids Res 29:137-140.
    • (2001) Nucleic Acids Res , vol.29 , pp. 137-140
    • Pruitt, K.D.1    Maglott, D.R.2
  • 17
    • 0031762950 scopus 로고    scopus 로고
    • GeneCards: A novel functional genomics compendium with automated data mining and query reformulation support
    • Rebhan M, Chalifa-Caspi V, Prilusky J, Lancet D. 1998. GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support. Bioinformatics 14:656-664.
    • (1998) Bioinformatics , vol.14 , pp. 656-664
    • Rebhan, M.1    Chalifa-Caspi, V.2    Prilusky, J.3    Lancet, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.