A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1-Reference-Cited by-同舟云学术

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A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1

Published:1996-08-01 Issue:8 Volume:5 Page:1193-1197
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Xu S.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/5/8/1193/8114994/5-8-1193.pdf

Cited by 25 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. Two Cases of Ocular Manifestations in Patients with Microdeletion of the Chromosome 7 Long Arm;Journal of the Korean Ophthalmological Society;2021-07-15

2. The role of splicing factors in retinitis pigmentosa: links to cilia;Biochemical Society Transactions;2021-06-01

3. PRPF3;Retinal Dystrophy Gene Atlas;2018

4. Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs;The American Journal of Human Genetics;2009-11

5. Association of a Novel Mutation in the Retinol Dehydrogenase 12 (RDH12) Gene With Autosomal Dominant Retinitis Pigmentosa;Archives of Ophthalmology;2008-09-08

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