- Tytuł:
- A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family.
- Autorzy:
- Źródło:
- Hereditas [Hereditas] 2024 Feb 20; Vol. 161 (1), pp. 9. Date of Electronic Publication: 2024 Feb 20.
- Typ publikacji:
- Journal Article
- MeSH Terms:
-
Afibrinogenemia*/genetics
Afibrinogenemia*/congenital
Afibrinogenemia*/diagnosis
Asian People*/geneticsFibrinogen */geneticsFibrinogen */chemistry
Humans ; China ; Mutation
Czasopismo naukowe