A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.
Int J Pediatr Otorhinolaryngol
; 107: 97-100, 2018 Apr.
Article
in En
| MEDLINE
| ID: mdl-29501320
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Membrane Transport Proteins
/
Vestibular Aqueduct
/
Deafness
/
Hearing Loss, Sensorineural
Limits:
Child
/
Female
/
Humans
/
Male
/
Newborn
Language:
En
Journal:
Int J Pediatr Otorhinolaryngol
Year:
2018
Document type:
Article
Affiliation country:
China
Country of publication:
Ireland