Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B).
NPJ Genom Med
; 7(1): 2, 2022 Jan 13.
Article
in En
| MEDLINE
| ID: mdl-35027574
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
NPJ Genom Med
Year:
2022
Document type:
Article
Affiliation country:
Reino Unido
Country of publication:
Reino Unido