Gerald Holder

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
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"Gerald Holder"
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Publications

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Ritter M, Arno G, Ba-Abbad R, et al. (2019) Macular maldevelopment in -mediated retinal dysfunction. Ophthalmic Genetics. 40: 564-569
Ku CA, Hull S, Arno G, et al. (2017) Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. Jama Ophthalmology
Hull S, Mukherjee R, Holder GE, et al. (2016) The clinical features of retinal disease due to a dominant mutation in RPE65. Molecular Vision. 22: 626-35
Arno G, Hull S, Robson AG, et al. (2015) Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 56: 2358-65
Hull S, Arno G, Plagnol V, et al. (2014) The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype. Investigative Ophthalmology & Visual Science. 55: 6934-44
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