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Case Reports
. 1992 Dec;1(9):767-8.
doi: 10.1093/hmg/1.9.767.

A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients

Z P Zhang  1 , G Falk, M Blombäck, N Egberg, M Anvret
Affiliations
Case Reports

A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients

Z P Zhang et al. Hum Mol Genet. 1992 Dec.
No abstract available

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