A novel nonsense mutation in the tyrosinase gene is related to the albinism in a capuchin monkey (Sapajus apella)

BACKGROUND: Oculocutaneous Albinism (OCA) is an autosomal recessive inherited condition that affects the pigmentation of eyes, hair and skin. The OCA phenotype may be caused by mutations in the tyrosinase gene (TYR), which expresses the tyrosinase enzyme and has an important role in the synthesis of...

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Bibliografiska uppgifter
I publikationen:BMC Genet
Huvudupphovsmän: Galante Rocha de Vasconcelos, Felipe Tadeu, Hauzman, Einat, Dutra Henriques, Leonardo, Kilpp Goulart, Paulo Roney, de Faria Galvão, Olavo, Sano, Ronaldo Yuiti, da Silva Souza, Givago, Lynch Alfaro, Jessica, de Lima Silveira, Luis Carlos, Fix Ventura, Dora, Oliveira Bonci, Daniela Maria
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2017
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5420114/
https://ncbi.nlm.nih.gov/pubmed/28476152
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12863-017-0504-8
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