Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B). (2022)
Attributed to:
Promoting Innovation and Collaboration: Translational Medicine in Exeter 2 (PICTME2)
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