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TULP1 Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

PURPOSE. To investigate visual function and outer and inner retinal structure in the rare form of retinal degeneration (RD) caused by TULP1 (tubby-like protein 1) mutations. METHODS. Retinal degeneration patients with TULP1 mutations (n = 5; age range, 5–36 years) were studied by kinetic and chromat...

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מידע ביבליוגרפי
הוצא לאור ב:	Invest Ophthalmol Vis Sci
Main Authors:	Jacobson, Samuel G., Cideciyan, Artur V., Huang, Wei Chieh, Sumaroka, Alexander, Roman, Alejandro J., Schwartz, Sharon B., Luo, Xunda, Sheplock, Rebecca, Dauber, Joanna M., Swider, Malgorzata, Stone, Edwin M.
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	The Association for Research in Vision and Ophthalmology 2014
נושאים:	Articles
גישה מקוונת:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4580213/ https://ncbi.nlm.nih.gov/pubmed/25074776 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.14-14570
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TULP1 Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

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