A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea-Reference-Cited by-同舟云学术

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A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Published:1993 Issue:5 Volume:2 Page:601-603
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Nichols B.E.,Drack A.V.,Vandenburgh K.,Kimura A.E.,Sheffield V.C.,Stone E.M.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/2/5/601/1783367/2-5-601.pdf

Cited by 66 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

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2. Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome data;BMC Genomics;2023-04-18

3. The pseudohypopyon stage in adult-onset foveomacular vitelliform dystrophy;International Ophthalmology;2023-04-17

4. New Insight into the Genotype-Phenotype Correlation of PRPH2-Related Diseases Based on a Large Chinese Cohort and Literature Review;International Journal of Molecular Sciences;2023-04-04

5. PRPH2 (RDS);Retinal Dystrophy Gene Atlas;2018

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