Identification of a novel nonsense mutation leading to congenital factor XIII deficiency.
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BORIS DOI
Publisher DOI
PubMed ID
29604433
Date of Publication
2018-05
Publication Type
Article
Subject(s)
Keyword(s)
Congenital factor XIII deficiency Cys327Stop F13A gene mutations Factor XIII Rare bleedings disorders
Language(s)
en
Contributor(s)
Borhany, Munira | |
Abid, Madiha |
Series
Thrombosis research
Publisher
Elsevier
ISSN
0049-3848
Access(Rights)
restricted