论文信息 - 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 - 字舞流文

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

B. George | A. Viswabandya | M. Chandy | G. Jayandharan | S. Nair | A. Srivastava | S. Baidya | R. V. Shaji | R. V. Shaji | S. Nair