Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype

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Title Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype
Creator Firuzeh Rajabian; Maria Pia Manitto; Flavia Palombo; Leonardo Caporali; Alessio Grazioli; Vincenzo Starace; Alessandro Arrigo; Maria Lucia Cascavilla; Chiara La Morgia; Piero Barboni; Francesco Bandello; Valerio Carelli; Maurizio Battaglia Parodi
Affiliation Vita-Salute San Raffaele University Milan (FR, MPM, AG, VS, AA, MLC, PB, FB, MBP), Milan, Italy; IRCCS San Raffaele Scientific Institute (FR, MPM, AG, VS, AA, MLC, PB, FB, MBP), Milan, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (FP, LC, CLM, VC), Bologna, Italy; and Department of Biomedical and Neuromotor Sciences (DIBINEM) (CLM, VC), University of Bologna, Bologna, Italy
Subject Carrier Proteins; Cone-Rod Dystrophies; Follow-Up Studies; Mitochondrial Proteins; Mutation; Optic Atrophy; Retinal Ganglion Cells; Rod Cell Outer Segmen; Time Factors; Optical Coherence Tomography; Visual Fields
OCR Text Show
Date 2021-09
Language eng
Format application/pdf
Type Text
Publication Type Journal Article
Source Journal of Neuro-Ophthalmology, September 2021, Volume 41, Issue 3
Collection Neuro-Ophthalmology Virtual Education Library: Journal of Neuro-Ophthalmology Archives: https://novel.utah.edu/jno/
Publisher Lippincott, Williams & Wilkins
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management © North American Neuro-Ophthalmology Society
ARK ark:/87278/s6wrfnn1
Setname ehsl_novel_jno
ID 2033170
Reference URL https://collections.lib.utah.edu/ark:/87278/s6wrfnn1
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