OCA7 is a melanosome membrane protein that defines pigmentation by regulating early stages of melanosome biogenesis

Mutations in C10orf11 (oculocutaneous albinism type 7 [OCA7]) cause OCA, a disorder that presents with hypopigmentation in skin, eyes, and hair. The OCA7 pathophysiology is unknown, and there is virtually no information on the OCA7 protein and its cellular function. Here, we discover that OCA7 local...

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Detalles Bibliográficos
Autores principales: Beyers, Wyatt C., Detry, Anna M., Di Pietro, Santiago M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703636/
https://www.ncbi.nlm.nih.gov/pubmed/36334630
http://dx.doi.org/10.1016/j.jbc.2022.102669

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703636/
https://www.ncbi.nlm.nih.gov/pubmed/36334630
http://dx.doi.org/10.1016/j.jbc.2022.102669

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