A novel case of compound heterozygosity with “Normandy”/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWD
Virginie Siguret, Jean-Maurice Lavergne, Ghislaine Chérel, Catherine Boyer-Neumann, Anne-Sophie Ribba, Bruce R. Bahnak, Dominique Meyer, Geneviève PiétuVolume:
93
Langue:
english
Pages:
8
DOI:
10.1007/bf00210590
Date:
February, 1994
Fichier:
PDF, 1.26 MB
english, 1994
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