Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss.
Int J Mol Sci
; 24(23)2023 Dec 03.
Article
in En
| MEDLINE
| ID: mdl-38069401
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Bartter Syndrome
/
Deafness
/
Alkalosis
/
Hearing Loss, Sensorineural
Limits:
Humans
Language:
En
Journal:
Int J Mol Sci
Year:
2023
Document type:
Article
Country of publication:
Switzerland