Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online.

Human mutation

Volumn 12, Issue 2, 1998, Pages 137-

  Klaus, D J ^a   Gallione, C J ^a   Anthony, K ^a   Yeh, E Y ^a   Yu, J ^a   Lux, A ^a   Johnson, D W ^a   Marchuk, D A ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN RECEPTOR; PROTEIN SERINE THREONINE KINASE; TRANSFORMING GROWTH FACTOR BETA RECEPTOR;

ARTICLE; CHROMOSOME 12; FRAMESHIFT MUTATION; GENETICS; HUMAN; MISSENSE MUTATION; RENDU OSLER WEBER DISEASE;

ACTIVIN RECEPTORS; CHROMOSOMES, HUMAN, PAIR 12; FRAMESHIFT MUTATION; HUMANS; MUTATION, MISSENSE; PROTEIN-SERINE-THREONINE KINASES; RECEPTORS, TRANSFORMING GROWTH FACTOR BETA; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

MLCS; MLOWN;

EID: 18744432185     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1998)12:2<137::aid-humu15>3.3.co;2-d     Document Type: Article

References (0)