![Frontiers | Genetic Analysis of 28 Chinese Families With Tyrosinase-Positive Oculocutaneous Albinism Frontiers | Genetic Analysis of 28 Chinese Families With Tyrosinase-Positive Oculocutaneous Albinism](https://www.frontiersin.org/files/Articles/715437/fgene-12-715437-HTML-r1/image_m/fgene-12-715437-g001.jpg)
Frontiers | Genetic Analysis of 28 Chinese Families With Tyrosinase-Positive Oculocutaneous Albinism
![Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers | Scientific Reports Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-021-01940-w/MediaObjects/41598_2021_1940_Fig1_HTML.png)
Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers | Scientific Reports
![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 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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fjhg.2009.130/MediaObjects/10038_2010_Article_BFjhg2009130_Fig3_HTML.jpg)
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
![Novel OCA2 mutations and resulting OCA2 phenotypes. A.Electropherograms... | Download Scientific Diagram Novel OCA2 mutations and resulting OCA2 phenotypes. A.Electropherograms... | Download Scientific Diagram](https://www.researchgate.net/publication/228069538/figure/fig7/AS:216453459517458@1428617934665/Novel-OCA2-mutations-and-resulting-OCA2-phenotypes-AElectropherograms-of-amplimers-from.png)
Novel OCA2 mutations and resulting OCA2 phenotypes. A.Electropherograms... | Download Scientific Diagram
![Genes | Free Full-Text | Delineating Novel and Known Pathogenic Variants in TYR, OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families Genes | Free Full-Text | Delineating Novel and Known Pathogenic Variants in TYR, OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families](https://www.mdpi.com/genes/genes-13-00503/article_deploy/html/images/genes-13-00503-g001.png)
Genes | Free Full-Text | Delineating Novel and Known Pathogenic Variants in TYR, OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families
![EVOLUTION OF EYE COLOR ELISE WOOD 11/20/2014. Ancestry of eye color What causes different shades to appear Mutation? Advantage? Large numbers. - ppt download EVOLUTION OF EYE COLOR ELISE WOOD 11/20/2014. Ancestry of eye color What causes different shades to appear Mutation? Advantage? Large numbers. - ppt download](https://images.slideplayer.com/20/5954909/slides/slide_6.jpg)
EVOLUTION OF EYE COLOR ELISE WOOD 11/20/2014. Ancestry of eye color What causes different shades to appear Mutation? Advantage? Large numbers. - ppt download
![Frontiers | Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort Frontiers | Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort](https://www.frontiersin.org/files/Articles/486128/fgene-11-00397-HTML/image_m/fgene-11-00397-g001.jpg)
Frontiers | Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort
![Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene](https://researcherslinks.com/uploads/currentIssues/figures/20220221052719.png)
Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene
![Genetic variation in regulatory DNA elements: the case of OCA2 transcriptional regulation - Visser - 2014 - Pigment Cell & Melanoma Research - Wiley Online Library Genetic variation in regulatory DNA elements: the case of OCA2 transcriptional regulation - Visser - 2014 - Pigment Cell & Melanoma Research - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/0798188f-b807-43f3-984a-3f7c8b4b003e/pcmr12210-fig-0002-m.jpg)
Genetic variation in regulatory DNA elements: the case of OCA2 transcriptional regulation - Visser - 2014 - Pigment Cell & Melanoma Research - Wiley Online Library
![Chromosome 15 (human) Mutations in the OCA2 gene cause a disruption in the normal production of melanin; therefore, … | Gene expression, Plasma membrane, Chromosome Chromosome 15 (human) Mutations in the OCA2 gene cause a disruption in the normal production of melanin; therefore, … | Gene expression, Plasma membrane, Chromosome](https://i.pinimg.com/originals/9c/b2/63/9cb263da6115b70dd08a18034cf14a34.png)