Genotype-phenotype correlations in multiple lesions of familial cerebral cavernous malformations concerning phosphatidylinositol 3-kinase catalytic subunit alpha mutations.

Subjects

Subjects :

Catalytic Domain
Genetic Association Studies
Mutation genetics
Phosphatidylinositol 3-Kinases genetics
Hemangioma, Cavernous, Central Nervous System

Details

Language :

English

ISSN :

2001-1326

Volume :

14

Issue :

3

Database :

MEDLINE

Journal :

Clinical and translational medicine

Publication Type :

Report

Accession number :

38450890

Full Text :

https://doi.org/10.1002/ctm2.1610