Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD.
NPJ Genom Med
; 6(1): 53, 2021 Jun 29.
Article
in En
| MEDLINE
| ID: mdl-34188062
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Diagnostic_studies
Language:
En
Journal:
NPJ Genom Med
Year:
2021
Document type:
Article
Affiliation country:
United States
Country of publication:
United kingdom