Hetero-oligomeric interactions of an ELOVL4 mutant protein: implications in the molecular mechanism of Stargardt-3 macular dystrophy

PURPOSE: Stargardt disease 3 (STGD3) is a juvenile macular dystrophy caused by mutations in the elongase of very long-chain fatty acids-like 4 (ELOVL4) gene, which encodes an elongase involved in the production of extremely long-chain fatty acids. The STGD3-related mutations cause production of C-te...

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Detalles Bibliográficos
Autores principales: Okuda, Ayaka, Naganuma, Tatsuro, Ohno, Yusuke, Abe, Kensuke, Yamagata, Maki, Igarashi, Yasuyuki, Kihara, Akio
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996883/
https://www.ncbi.nlm.nih.gov/pubmed/21139992

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996883/
https://www.ncbi.nlm.nih.gov/pubmed/21139992

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