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

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Abstract
Kimberly A. McAllister, Melanie A. Baldwin, Arun K. Thukkani, Carol J. Gallione, Jonathan N. Berg, Mary E. Porteous, Allan E. Guttmacher, Douglas A. Marchuk; S