Rhodopsin mutations in autosomal dominant retinitis pigmentosa-Reference-Cited by-同舟云学术

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

Published:1993 Issue:4 Volume:2 Page:249-255
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Al-Maghtheh Mai,Gregory Cheryl,Inglehearn Chris,Hardcastle Alison,Bhattacharya Shomi

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference46 articles.

1. (1992) Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with Pro-347-Leu mutation of rhodopsin. German J Ophthalmol (in press).

2. Rhodopsin in the rod outer segment plasma membrane.

3. Temporal Aspects of the Electroretinogram in Sector Retinitis Pigmentosa

4. Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)

5. Prevalence of Retinitis Pigmentosa in Maine

Cited by 68 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. Genotype and phenotype characteristics of RHO-associated retinitis pigmentosa in the Japanese population;Japanese Journal of Ophthalmology;2023-01-17

2. Multimodal Imaging Characteristics of ADRP in a Family with p.Thr58Arg Substituted RHO Mutation;Case Reports in Genetics;2020-12-02

3. Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort;Journal of Ophthalmology;2020-10-06

4. Zebrafish Photoreceptor Degeneration and Regeneration Research to Understand Hereditary Human Blindness;Visual Impairment and Blindness - What We Know and What We Have to Know;2020-09-09

5. Human eye conditions: insights from the fly eye;Human Genetics;2018-11-01