✦ LIBER ✦
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
✍ Scribed by G. JAYANDHARAN; M. SPREAFICO; A. VISWABANDYA; M. CHANDY; A. SRIVASTAVA; F. PEYVANDI
- Book ID
- 108772794
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 448 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1351-8216
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