Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516TG factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin-Reference-Cited by-同舟云学术

Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516TG factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin

Published:2005-07 Issue:7 Volume:3 Page:1482-1487
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

JAYANDHARAN G.,VISWABANDYA A.,BAIDYA S.,NAIR S. C.,SHAJI R. V.,GEORGE B.,CHANDY M.,SRIVASTAVA A.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2005.01339.x/fullpdf

Reference30 articles.

1. Factor X and its deficiency states

2. Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)

3. Rare coagulation deficiencies

4. Inherited Factor X Deficiency: Molecular Genetics and Pathophysiology

5. Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency

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