(Q38326297)
Statements
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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 (English)
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Jayandharan G
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Viswabandya A
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Baidya S
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Nair SC
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Shaji RV
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George B
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Chandy M
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Srivastava A
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9 May 2005
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3
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7
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1482-1487
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Identifiers
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