Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon.
Mol Genet Genomic Med
; 9(3): e1609, 2021 03.
Article
in En
| MEDLINE
| ID: mdl-33528103
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Frameshift Mutation
/
Glutaredoxins
/
Hearing Loss
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Female
/
Humans
/
Male
Country/Region as subject:
Africa
Language:
En
Journal:
Mol Genet Genomic Med
Year:
2021
Document type:
Article
Affiliation country:
Sudáfrica
Country of publication:
Estados Unidos