✦ LIBER ✦
A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand’s disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation
✍ Scribed by M. S. ENAYAT; A. M. GUILLIATT; P. E. SHORT; G. RASTEGAR-LARI; M. JAZEBI; S. RAVONBOD; F. ALA; O. G. CHAPMAN; F. G. H. HILL
- Book ID
- 108775501
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 57 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1351-8216
No coin nor oath required. For personal study only.