Gln52 mutations in GNAO1-related disorders and personalized drug discovery

Subjects

Subjects :

GNAO1
Pediatric encephalopathy
G protein
Missense mutations
Animal models
Drug discovery
Neurology. Diseases of the nervous system
RC346-429
Neurophysiology and neuropsychology
QP351-495

Details

Language :

English

ISSN :

25899864

Volume :

24

Issue :

100598-

Database :

Directory of Open Access Journals

Journal :

Epilepsy & Behavior Reports

Publication Type :

Academic Journal

Accession number :

edsdoj.62a917fd4ce49c9c6c51496c460f

Document Type :

article

Full Text :

https://doi.org/10.1016/j.ebr.2023.100598