AUTOSOMAL DOMINANT CONE-ROD DYSTROPHY ASSOCIATED WITH A VAL200GLU MUTATION OF THE PERIPHERIN/RDS GENE-Reference-Cited by-同舟云学术

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AUTOSOMAL DOMINANT CONE-ROD DYSTROPHY ASSOCIATED WITH A VAL200GLU MUTATION OF THE PERIPHERIN/RDS GENE

Published:1996 Issue:5 Volume:16 Page:405-410
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:Retina

Author:

NAKAZAWA MITSURU,NAOI NOBUHISA,WADA YUKO,NAKAZAKI SHUJI,MARUIWA FUTOSHI,SAWADA ATSUSHI,TAMAI MAKOTO

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Cited by 32 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. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes;Progress in Retinal and Eye Research;2024-05

2. Progressive and Stationary Disorders of Cone Function: Cone and Cone-Rod Dystrophies and Cone Dysfunction Syndromes;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

3. Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan;Genes;2021-11-18

4. PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal disease;Human Mutation;2021-09-20

5. Progressive and Stationary Disorders of Cone Function: Cone and Cone-Rod Dystrophies and Cone Dysfunction Syndromes;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021

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