Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models

Mutations in the Retinitis Pigmentosa GTPase Regulator (RPGR) cause X-linked RP (XLRP), an untreatable, inherited retinal dystrophy that leads to premature blindness. RPGR localises to the photoreceptor connecting cilium where its function remains unknown. Here we show, using murine and human induce...

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Detalles Bibliográficos
Autores principales: Megaw, Roly, Abu-Arafeh, Hashem, Jungnickel, Melissa, Mellough, Carla, Gurniak, Christine, Witke, Walter, Zhang, Wei, Khanna, Hemant, Mill, Pleasantine, Dhillon, Baljean, Wright, Alan F., Lako, Majlinda, ffrench-Constant, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559447/
https://www.ncbi.nlm.nih.gov/pubmed/28814713
http://dx.doi.org/10.1038/s41467-017-00111-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559447/
https://www.ncbi.nlm.nih.gov/pubmed/28814713
http://dx.doi.org/10.1038/s41467-017-00111-8

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