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Mitochondrial NCKX5 regulates melanosomal biogenesis and pigment production
Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive hypopigmentation disorder, which is caused by mutations of genes involved in pigment biosynthesis or melanosome biogenesis. We have previously identified NCKX5 (also known as SLC24A5) as a causative gene for OCA type 6 (OCA6)....
Tallennettuna:
| Julkaisussa: | J Cell Sci |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Company of Biologists Ltd
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6679581/ https://ncbi.nlm.nih.gov/pubmed/31201282 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.232009 |
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