SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect.
Brain
; 143(8): 2380-2387, 2020 08 01.
Article
in En
| MEDLINE
| ID: mdl-32658972
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Solute Carrier Family 12, Member 2
/
Neurodevelopmental Disorders
/
Bilateral Vestibulopathy
/
Hearing Loss, Sensorineural
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Brain
Year:
2020
Type:
Article
Affiliation country:
United kingdom