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Article

Clinical significance of two mutations in the factor IX gene in a family with haemophilia B.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Mar 2010

Sexton A, Furmedge J, Barnes C, Cheetham G, Wallace J, Savarirayan R

Abstract excerpt

No abstract is available from the source.

Topics

DNA Mutational Analysis
Exons
Factor IX
Female
Genetic Testing
Hemophilia B
Humans
Male
Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19930472
DOI: 10.1111/j.1365-2516.2009.02143.x

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