A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet-Biedl syndrome.
Int Ophthalmol
; 41(2): 389-397, 2021 Feb.
Article
in En
| MEDLINE
| ID: mdl-32926352
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Autoantigens
/
Bardet-Biedl Syndrome
/
Neoplasm Proteins
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Int Ophthalmol
Year:
2021
Document type:
Article
Affiliation country: