TULP1Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones | Zendy

Samuel G. Jacobson | Zendy; Artur V. Cideciyan | Zendy; Wei Huang | Zendy; Alexander Sumaroka | Zendy; Alejandro J. Román | Zendy; Sharon Schwartz | Zendy; Xunda Luo | Zendy; Rebecca Sheplock | Zendy; Joanna M. Dauber | Zendy; Małgorzata Świder | Zendy; Edwin M. Stone | Zendy

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TULP1Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

Author(s) -

Samuel G. Jacobson,

Artur V. Cideciyan,

Wei Huang,

Alexander Sumaroka,

Alejandro J. Román,

Sharon Schwartz,

Xunda Luo,

Rebecca Sheplock,

Joanna M. Dauber,

Małgorzata Świder,

Edwin M. Stone

Publication year - 2014

Publication title -

investigative ophthalmology and visual science

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.935

H-Index - 218

eISSN - 1552-5783

pISSN - 0146-0404

DOI - 10.1167/iovs.14-14570

Subject(s) - retinal , retinal degeneration , retinal pigment epithelium , retina , foveal , ophthalmology , retinitis pigmentosa , macular degeneration , fovea centralis , biology , autofluorescence , electroretinography , anatomy , medicine , optics , neuroscience , physics , fluorescence

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.

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