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.
(Q38311695)
scientific article published on February 1994
scientific article published on February 1994
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| description | scientific article published on February 1994 |
External Links
| (P356) |
10.1007/BF00210590
|
| (P698) |
7906671
|
| (P6179) |
1006294144
|