Novel human pathological mutations. Gene symbol: F13A1. Disease: Factor XIII Deficiency
Hum Genet
.
2010 Jan;127(1):115-6.
Authors
Rashida Anwar
1
,
Elizabeth M A Valleley
,
Chi H Trinh
Affiliation
1
Leeds Institute of Molecular Medicine, University of Leeds, St James's University Hospital, Beckett Street, LS9 7TF, Leeds, United Kingdom.
[email protected]
PMID:
20108427
No abstract available
MeSH terms
Codon / genetics
Factor XIII Deficiency / genetics*
Factor XIIIa / genetics*
Humans
Mutation, Missense*
Substances
Codon
Factor XIIIa