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Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor function

Kimberly A. McAllister, Jonathan Berg, Mary Porteous, Allan E. Guttmacher, Melanie A. Baldwin
DOI: 10.1093/hmg/4.10.1983
Human Molecular Genetics

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Published1995
Citations109
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Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1… (1995) – Human Molecular Genetics | Metascience Observatory Explorer