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Localization to Mature Melanosomes by Virtue of Cytoplasmic Dileucine Motifs Is Required for Human OCA2 Function

Oculocutaneous albinism type 2 is caused by defects in the gene OCA2, encoding a pigment cell-specific, 12-transmembrane domain protein with homology to ion permeases. The function of the OCA2 protein remains unknown, and its subcellular localization is under debate. Here, we show that endogenous OC...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Sitaram, Anand, Piccirillo, Rosanna, Palmisano, Ilaria, Harper, Dawn C., Dell'Angelica, Esteban C., Schiaffino, M. Vittoria, Marks, Michael S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The American Society for Cell Biology 2009
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2649270/
https://ncbi.nlm.nih.gov/pubmed/19116314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E08-07-0710
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