Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations

American Journal of Human Genetics

Volumn 63, Issue 2, 1998, Pages 380-389

  Monreal, Alex W ^a   Zonana, Jonathan ^a   Ferguson, Betsy ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ISOPROTEIN; M PROTEIN;

ARTICLE; GENE ISOLATION; GENE MUTATION; GENE STRUCTURE; HETEROZYGOTE DETECTION; HUMAN; HYPOHIDROTIC ECTODERMAL DYSPLASIA; MALE; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; RNA SPLICING; TOOTH DEVELOPMENT; X CHROMOSOME LINKAGE;

MURINAE;

EID: 0032231350     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301984     Document Type: Article

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