✦ LIBER ✦
Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: Definite evidence for the non-penetrance of the C2362F mutation
✍ Scribed by G. Castaman; K. Bertoncello; M. Bernardi; J.C.J. Eikenboom; U. Budde; F. Rodeghiero
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 196 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0361-8609
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