✦ LIBER ✦
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T→G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin
✍ Scribed by G. JAYANDHARAN; A. VISWABANDYA; S. BAIDYA; S. C. NAIR; R. V. SHAJI; B. GEORGE; M. CHANDY; A. SRIVASTAVA
- Book ID
- 118714713
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 193 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1538-7933
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