Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 families.
Gene
; 894: 147986, 2024 Feb 05.
Article
in En
| MEDLINE
| ID: mdl-37956964
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Albinism, Oculocutaneous
Limits:
Humans
Language:
En
Journal:
Gene
Year:
2024
Document type:
Article
Affiliation country:
Pakistan
Country of publication:
Netherlands