Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A
Published inThrombosis Research, vol. 193, p. 5-8
Publication date2020
Citation (ISO format)
FERREIRA VILAR DA SILVA, Rui Filipe et al. Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A. In: Thrombosis Research, 2020, vol. 193, p. 5–8. doi: 10.1016/j.thromres.2020.05.040
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Article (Published version)
Identifiers
- PID : unige:139625
- DOI : 10.1016/j.thromres.2020.05.040
- PMID : 32497950
ISSN of the journal0049-3848
