Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
J Mol Diagn
; 23(10): 1279-1291, 2021 10.
Article
in En
| MEDLINE
| ID: mdl-34325055
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Alleles
/
Usher Syndromes
/
Connexin 26
/
Hearing Loss, Sensorineural
/
Heterozygote
/
Homozygote
Type of study:
Prognostic_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
J Mol Diagn
Year:
2021
Document type:
Article