Genetic variation in regulatory DNA elements: the case of OCA2 transcriptional regulation - Visser - 2014 - Pigment Cell & Melanoma Research - Wiley Online Library
Albinism, Oculocutaneous, Type II | Hereditary Ocular Diseases
HERC2 and OCA2: how blue-eyed is the perpetrator? - The Gene of the Week.
Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene
![PDF] Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/6db35eeebbf3bd11b94a9860317c72e0d4b1814c/3-Figure2-1.png "PDF] Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree. | Semantic Scholar")
PDF] Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree. | Semantic Scholar
Sandwalk: Human OCA2 Gene Is Responsible for Eye Color and Skin Color
Frontiers | Genetic Analysis of 28 Chinese Families With Tyrosinase-Positive Oculocutaneous Albinism
Eye Colour Genes and Genetics – Genetic Education
oca2 – thatbiologist
OCA2 - an overview | ScienceDirect Topics
Oculocutaneous Albinism - an overview | ScienceDirect Topics
OCA2 Melanosomal Transmembrane Protein (OCA2) Antibody | Abbexa Ltd
GB Lifesciences
Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community | Journal of Human Genetics
OCA2 - Wikipedia
OCA2 Gene - GeneCards | P Protein | P Antibody
OCA2 Gene - GeneCards | P Protein | P Antibody
![PDF] Eye colour: portals into pigmentation genes and ancestry. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/160750e7274a0d10862d8af55c79b8bb08de46ed/1-Figure1-1.png "PDF] Eye colour: portals into pigmentation genes and ancestry. | Semantic Scholar")
PDF] Eye colour: portals into pigmentation genes and ancestry. | Semantic Scholar
OCA2 Gene | Thasso
Genes | Free Full-Text | Delineating Novel and Known Pathogenic Variants in TYR, OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families
Chromosome 15 (human) Mutations in the OCA2 gene cause a disruption in the normal production of melanin; therefore, … | Gene expression, Plasma membrane, Chromosome
Sequencing results of TYR gene (patient A,C and D)or OCA2 gene(patient... | Download Scientific Diagram
A novel porcine model reproduces human oculocutaneous albinism type II | Cell Discovery
Debunking another "We are not Albinos" study
Novel OCA2 mutations and resulting OCA2 phenotypes. A.Electropherograms... | Download Scientific Diagram
DNA sequencing result from OCA2 gene (a-c) or TYR (d) gene.... | Download Scientific Diagram
File:OCA2 location.png - Wikimedia Commons
Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers | Scientific Reports
