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Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.
Johnson, D W; Berg, J N; Baldwin, M A; Gallione, C J; Marondel, I; Yoon, S J; Stenzel, T T; Speer, M; Pericak-Vance, M A; Diamond, A; Guttmacher, A E; Jackson, C E; Attisano, L; Kucherlapati, R; Porteous, M E; Marchuk, D A.
Affiliation
  • Johnson DW; Department of Genetics, Duke University Medical Center, Durham, North Carolina 27710, USA.
Nat Genet ; 13(2): 189-95, 1996 Jun.
Article in En | MEDLINE | ID: mdl-8640225
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Collection: 01-internacional Database: MEDLINE Main subject: Telangiectasia, Hereditary Hemorrhagic / Chromosomes, Human, Pair 12 / Protein Serine-Threonine Kinases / Mutation Limits: Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Telangiectasia, Hereditary Hemorrhagic / Chromosomes, Human, Pair 12 / Protein Serine-Threonine Kinases / Mutation Limits: Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: United States Country of publication: United States