A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotype.
Ann Neurol
; 83(2): 437-439, 2018 02.
Article
in En
| MEDLINE
| ID: mdl-29369404
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Rett Syndrome
Limits:
Humans
Language:
En
Journal:
Ann Neurol
Year:
2018
Document type:
Article