Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B). (2022)

First Author: Lin S
Attributed to:  Precision Medicine Exeter Innovation Platform (PMEI Platform) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41525-021-00275-9

PubMed Identifier: 35027574

Publication URI: http://europepmc.org/abstract/MED/35027574

Type: Journal Article/Review

Volume: 7

Parent Publication: NPJ genomic medicine

Issue: 1

ISSN: 2056-7944