✦ LIBER ✦
Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362→Thr (Prothrombin Vellore 1) mutation
✍ Scribed by G. JAYANDHARAN; A. VISWABANDYA; S. BAIDYA; S. C. NAIR; R. V. SHAJI; M. CHANDY; A. SRIVASTAVA
- Book ID
- 109149047
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 257 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1538-7933
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