Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF.
BMC Med Genet
; 21(1): 1, 2020 01 02.
Article
in En
| MEDLINE
| ID: mdl-31898538
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myosins
/
Genetic Heterogeneity
/
Microphthalmia-Associated Transcription Factor
/
Hearing Loss, Sensorineural
Type of study:
Prognostic_studies
Limits:
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
BMC Med Genet
Journal subject:
GENETICA MEDICA
Year:
2020
Document type:
Article
Affiliation country:
Country of publication: