Clinical significance of two mutations in the factor IX gene in a family with haemophilia B
Haemophilia
.
2010 Mar;16(2):374-6.
doi: 10.1111/j.1365-2516.2009.02143.x.
Epub 2009 Nov 23.
Authors
A Sexton
,
J Furmedge
,
C Barnes
,
G Cheetham
,
J Wallace
,
R Savarirayan
PMID:
19930472
DOI:
10.1111/j.1365-2516.2009.02143.x
No abstract available
Publication types
Case Reports
Letter
MeSH terms
DNA Mutational Analysis
Exons / genetics
Factor IX / genetics*
Female
Genetic Testing
Hemophilia B / genetics*
Humans
Male
Mutation*
Substances
Factor IX