- Tytuł:
- Genotype-phenotype correlations in multiple lesions of familial cerebral cavernous malformations concerning phosphatidylinositol 3-kinase catalytic subunit alpha mutations.
- Autorzy:
- Źródło:
- Clinical and translational medicine [Clin Transl Med] 2024 Mar; Vol. 14 (3), pp. e1610.
- Typ publikacji:
- Letter; Research Support, Non-U.S. Gov't
- MeSH Terms:
-
Phosphatidylinositol 3-Kinases*/genetics
Hemangioma , Cavernous, Central Nervous System*
Catalytic Domain ; Genetic Association Studies ; Mutation/genetics - SCR Disease Name:
- Familial cerebral cavernous malformation
Raport