New compound heterozygous USH2A mutations in Usher syndrome.
Acta Ophthalmol
; 98(1): e134-e135, 2020 Feb.
Article
in En
| MEDLINE
| ID: mdl-30390381
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
DNA
/
Extracellular Matrix Proteins
/
Usher Syndromes
/
Mutation
Type of study:
Diagnostic_studies
Limits:
Adult
/
Female
/
Humans
Language:
En
Journal:
Acta Ophthalmol
Journal subject:
OFTALMOLOGIA
Year:
2020
Document type:
Article
Affiliation country:
China