Mutational epidemiology of congenital fibrinogen disorders
Published inThrombosis and Haemostasis, vol. 118, no. 11, p. 1867-1874
Publication date2018
Abstract
Keywords
- Adolescent
- Adult
- Afibrinogenemia/epidemiology/genetics
- Alleles
- Child
- Child, Preschool
- DNA Mutational Analysis
- Female
- Fibrinogen/genetics
- Genetic Testing
- Genotype
- Hemostasis/genetics
- Humans
- Male
- Molecular Epidemiology
- Mutation/genetics
- Prospective Studies
- Switzerland/epidemiology
- Young Adult
Funding
- Swiss National Science Foundation - 31003A-152633/I
- Swiss National Science Foundation - Molecular mechanisms and clinical consequences of variable fibrinogen levels [31003A_172864]
Citation (ISO format)
CASINI, Alessandro et al. Mutational epidemiology of congenital fibrinogen disorders. In: Thrombosis and Haemostasis, 2018, vol. 118, n° 11, p. 1867–1874. doi: 10.1055/s-0038-1673685
Main files (2)
Article (Accepted version)
Article (Published version)
Identifiers
- PID : unige:115121
- DOI : 10.1055/s-0038-1673685
- PMID : 30332696
ISSN of the journal0340-6245