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albinism, oculocutaneous, type ii
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OCA2
Absence of predictable phenotypic expression in proximal 15q duplications
Organization and sequence of the human P gene and identification of a new family of transport proteins
Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2)
TYRP1
Human tyrosinase-like protein (TYRL) carboxy terminus: closer homology with the mouse protein than previously reported
Nucleotide sequence of the cDNA encoding human tyrosinase-related protein
The melanoma antigen gp75 is the human homologue of the mouse b (brown) locus gene product
MC1R
Melanocortin-1 Receptor Polymorphisms and the Risk of Complicated Sepsis After Trauma: A Candidate Gene Association Study
Skin phototype: a new perspective
Single-nucleotide polymorphisms in pigment genes and nonmelanoma skin cancer predisposition: a systematic review
Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma
Basal cell carcinoma, squamous cell carcinoma and melanoma of the head and face
Cancer Gene Census
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Definition
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Pathways
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Melanogenesis
Homo sapiens (human)
2 genes
Clinical Trials
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External
Role of Gastrointestinal Microbes on Digestion of Resistant Starch and Tryptophan Availability to Humans