Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (Ile865 to Thr)

American Journal of Human Genetics

Volumn 48, Issue 4, 1991, Pages 757-763

  Iannuzzi, M C ^a   Hidaka, N ^a   Boehnke, M ^a   Bruck, M E ^a   Hanna, W T ^a   Collins, F S ^a   Ginsburg, D ^a  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 12; CLINICAL ARTICLE; FEMALE; GENE LOCATION; GENETIC LINKAGE; HUMAN; MALE; MUTATION; PEDIGREE; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; TELANGIECTASIA; VON WILLEBRAND DISEASE;

ALLELES; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 12; DNA; FEMALE; HUMAN; ISOLEUCINE; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; TELANGIECTASIA, HEREDITARY HEMORRHAGIC; THREONINE; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 0025821804     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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