Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa-Reference-Cited by-同舟云学术

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Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa

Published:2016-09 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Yang Yin,Yang Yeming,Huang Lulin,Zhai Yaru,Li Jie,Jiang Zhilin,Gong Bo,Fang Hao,Kim Ramasamy,Yang Zhenglin,Sundaresan Periasamy,Zhu Xianjun,Zhou Yu

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep33681.pdf

Reference35 articles.

1. Bird, A. C. Retinal photoreceptor dystrophies LI. Edward Jackson Memorial Lecture. Am J Ophthalmol 119, 543–562 (1995).

2. Rivolta, C., Sharon, D., DeAngelis, M. M. & Dryja, T. P. Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns. Hum Mol Genet 11, 1219–1227 (2002).

3. Bhatti, M. T. Retinitis pigmentosa, pigmentary retinopathies, and neurologic diseases. Curr Neurol Neurosci Rep 6, 403–413 (2006).

4. Hartong, D. T., Berson, E. L. & Dryja, T. P. Retinitis pigmentosa. Lancet 368, 1795–1809 (2006).

5. Ng, S. B. et al. Targeted capture and massively parallel sequencing of 12 human exomes. Nature 461, 272–276 (2009).

Cited by 6 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. Identification of a novel homozygous nonsense mutation in the CDHR1 gene in a Chinese family with autosomal recessive retinitis pigmentosa;Clinica Chimica Acta;2020-08

2. A Review on the Challenges in Indian Genomics Research for Variant Identification and Interpretation;Frontiers in Genetics;2020-07-22

3. Genomic Approaches to Eye Diseases: An Asian Perspective;Essentials in Ophthalmology;2018-11-04

4. Genetics and Susceptibility of Retinal Eye Diseases in India;Essentials in Ophthalmology;2018-11-04

5. Whole exome sequencing: Uncovering causal genetic variants for ocular diseases;Experimental Eye Research;2017-11

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