TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations.
Sci Rep
; 9(1): 12047, 2019 08 19.
Article
in En
| MEDLINE
| ID: mdl-31427709
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Eye Diseases, Hereditary
/
Night Blindness
/
Genetic Predisposition to Disease
/
Genetic Diseases, X-Linked
/
TRPM Cation Channels
/
Genetic Association Studies
/
Genes, Recessive
/
Mutation
/
Myopia
Type of study:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Sci Rep
Year:
2019
Document type:
Article
Affiliation country:
Country of publication: