SLC7A14 linked to autosomal recessive retinitis pigmentosa-Reference-Cited by-同舟云学术

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SLC7A14 linked to autosomal recessive retinitis pigmentosa

Published:2014-03-27 Issue:1 Volume:5 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Jin Zi-Bing,Huang Xiu-Feng,Lv Ji-Neng,Xiang Lue,Li Dong-Qing,Chen Jiangfei,Huang Changjiang,Wu Jinyu,Lu Fan,Qu Jia

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms4517.pdf

Reference23 articles.

1. Daiger, S., Sullivan, L. & Bowne, S. Genes and mutations causing retinitis pigmentosa. Clin. Genet. 84, 132–141 (2013).

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

3. Huang, X. F. et al. Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families. PLoS One 8, e63832 (2013).

4. Li, R. et al. SOAP2: an improved ultrafast tool for short read alignment. Bioinformatics 25, 1966–1967 (2009).

5. Jin, Z. B. et al. Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs. Invest. Ophthalmol. Vis. Sci. 49, 3799–3805 (2008).

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