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Article

Spectrum of factor IX gene mutations causing haemophilia B from India.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jul 2009

Ghosh Kanjaksha, Quadros Leera, Shetty Shrimati

Abstract excerpt

Haemophilia B is an X-linked recessively inherited disease caused by highly heterogeneous mutations in the factor IX gene. Very few studies are available on the nature of mutations in haemophilia B patients from India. The present study was undertaken with an aim to characterize the mutations present in haemophilia B patients from western India. The screening for mutations was done by conformation sensitive gel...

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PMID: 19357501
DOI: 10.1097/MBC.0b013e32832b27d1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

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