Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type

Nature Genetics

Volumn 13, Issue 2, 1996, Pages 189-195

  Johnson, D W ^a   Berg, J N ^a,b   Baldwin, M A ^a   Gallione, C J ^a   Marondel, I ^c   Yoon, S J ^c   Stenzel, T T ^a   Speer, M ^a   Pericak Vance, M A ^a   Diamond, A ^d   Guttmacher, A E ^e   Jackson, C E ^f   Attisano, L ^g   Kucherlapati, R ^c   Porteous, M E M ^b   Marchuk, D A ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d NEWCASTLE UNIVERSITY   (United Kingdom)

^e UNIVERSITY OF VERMONT   (United States)

^f HENRY FORD HOSPITAL   (United States)

^g UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN;

ANGIODYSPLASIA; ARTICLE; CHROMOSOME 12; CHROMOSOME 9Q; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; HUMAN; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE;

ACTIVIN RECEPTORS; AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PROTEIN-SERINE-THREONINE KINASES; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 0030050973     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0696-189     Document Type: Article

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