Mild haemophilia A in a female patient with a large X-chromosomal deletion and a missense mutation in the F8 gene--a case report
Haemophilia
.
2013 Sep;19(5):e310-3.
doi: 10.1111/hae.12190.
Epub 2013 May 28.
Authors
S Rost
,
V Aumann
,
I Nanda
,
J Oldenburg
,
C R Müller
PMID:
23710598
DOI:
10.1111/hae.12190
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child
Chromosome Deletion*
Chromosomes, Human, X*
Factor VIII / genetics*
Female
Hemophilia A / genetics*
Humans
Mutation, Missense*
Substances
Factor VIII