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Article

Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing.

Thrombosis research - 1 Jan 2007

Karimipoor Morteza, Zeinali Sirous, Nafissi Nafiseh, Tuddenham Edward G D, Lak Manijeh, Safaee Reza

Abstract excerpt

Different kinds of mutations, mostly point mutations, in the coagulation factor IX (FIX) gene F9 result in a recessive X-linked bleeding disorder known as haemophilia B. In this study, molecular analysis of 76 unrelated Iranian haemophilia B patients was performed by PCR, single strand conformational polymorphism (SSCP) on important functional regions of the F9 gene followed by sequencing on samples with...

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Identifiers

PMID: 17014892
DOI: 10.1016/j.thromres.2006.07.011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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