Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1)
Author:
Affiliation:
1. Department of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA
2. Retina Foundation of the Southwest, Dallas, TX, USA
3. Department of Ophthalmology, UT Southwestern Medical Center, Dallas, TX, USA
Publisher
Association for Research in Vision and Ophthalmology (ARVO)
Subject
Ophthalmology,Biomedical Engineering
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. IMPDH1 -associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search;Ophthalmic Genetics;2023-05-31
2. Disease progression of retinitis pigmentosa caused by PRPF31 variants in a Nordic population: a retrospective study with up to 36 years follow-up;Ophthalmic Genetics;2022-09-26
3. Genetic treatment for autosomal dominant inherited retinal dystrophies: approaches, challenges and targeted genotypes;British Journal of Ophthalmology;2022-08-29
4. Genetic dissection of non-syndromic retinitis pigmentosa;Indian Journal of Ophthalmology;2022
5. Retinitis Pigmentosa;Inherited Retinal Disease;2022
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