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Figure 2 Results of molecular investigations in the original family S in the 1990s reveal a heterozygous nonsense mutation in seven affected members with mild bleeding diathesis[4].
- Citation: Gadisseur A, Berneman Z, Schroyens W, Michiels JJ. Pseudohemophilia of Erik von Willebrand caused by homozygous one nucleotide deletion in exon 18 of the VW-factor gene. World J Hematol 2013; 2(4): 99-108
- URL: https://www.wjgnet.com/2218-6204/full/v2/i4/99.htm
- DOI: https://dx.doi.org/10.5315/wjh.v2.i4.99