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Article

[Mutational Analysis of Hemophilia B in Russia: Molecular-Genetic Study].

Genetika - 1 Apr 2016

Surin V L, Demidova E Yu, Selivanova D S, Luchinina Yu A, Salomashkina V V, Pshenichnikova O S, Likhacheva E A

Abstract excerpt

Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long and consisting of eight exons, localized in the Xq27 locus of the. X-chromosome long arm. Mutations were revealed in 56 unrelated patients with hemophilia B in this study by using direct sequencing of factor IX gene functionally important fragments....

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Identifiers

PMID: 27529981

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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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