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Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations

Autor: Tomas S. Aleman, Sharon B. Schwartz, Artur V. Cideciyan, Alejandro J. Roman, David B. McGuigan, Samuel G. Jacobson, Judy Palma, Alexander Sumaroka, Michaela L. Gruzensky, Rebecca Sheplock

Publikováno v: Investigative Ophthalmology & Visual Science

Purpose Previously, patients with RHO mutations and a class A phenotype were found to have severe early-onset loss of rod function, whereas patients with a class B phenotype retained rod function at least in certain retinal regions. Here class B pati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2ae646ecc7d968e906aed7bcb530a7
http://europepmc.org/articles/PMC5032913

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