Comprehensive Screening of Genetic Variants in the Coding Region of
F8
FVIII
hemophilia A
inhibitors
mutation
pathogenic
variants
whole sequence exome
Journal
Life (Basel, Switzerland)
ISSN: 2075-1729
Titre abrégé: Life (Basel)
Pays: Switzerland
ID NLM: 101580444
Informations de publication
Date de publication:
21 Aug 2024
21 Aug 2024
Historique:
received:
22
07
2024
revised:
08
08
2024
accepted:
15
08
2024
medline:
31
8
2024
pubmed:
31
8
2024
entrez:
29
8
2024
Statut:
epublish
Résumé
Hemophilia A is an X-linked disorder characterized by quantitative deficiency of coagulation factor VIII (FVIII) caused by pathogenic variants in the factor 8 (
Identifiants
pubmed: 39202783
pii: life14081041
doi: 10.3390/life14081041
pmc: PMC11355106
pii:
doi:
Types de publication
Journal Article
Langues
eng
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