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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): Proof of Concept Funds 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

Parent Publication: npj Genomic Medicine

Issue: 1

ISSN: 2056-7944