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Volumn 146, Issue 4, 2002, Pages 601-608

The hairless gene in androgenetic alopecia: Results of a systematic mutation screening and a family-based association approach

Author keywords

Genetic variation; Linkage disequilibrium; Male pattern baldness

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; EXON; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HAIRLESS GENE; HUMAN; MALE; MALE TYPE ALOPECIA; MISSENSE MUTATION; PRIORITY JOURNAL; SCREENING TEST; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0036239579     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2133.2002.04766.x     Document Type: Article
Times cited : (16)

References (21)
  • 10
    • 7344229369 scopus 로고    scopus 로고
    • Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal-recessive universal congenital alopecia
    • (1998) Hum Mol Genet , vol.7 , pp. 1671-1679
    • Cichon, S.1    Anker, M.2    Vogt, I.R.3
  • 19
    • 0032231885 scopus 로고    scopus 로고
    • A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers
    • (1998) Am J Hum Genet , vol.63 , pp. 984-991
    • Ahmad, W.1    Irvine, A.D.2    Lam, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.