PRPF4 mutations cause autosomal dominant retinitis pigmentosa-Reference-Cited by-同舟云学术

PRPF4 mutations cause autosomal dominant retinitis pigmentosa

Published:2014-01-12 Issue:11 Volume:23 Page:2926-2939
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Chen Xue,Liu Yuan,Sheng Xunlun,Tam Pancy O. S.,Zhao Kanxing,Chen Xuejuan,Rong Weining,Liu Yani,Liu Xiaoxing,Pan Xinyuan,Chen Li Jia,Zhao Qingshun,Vollrath Douglas,Pang Chi Pui,Zhao Chen

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/23/11/2926/13917757/ddu005.pdf

Reference54 articles.

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2. Good epidemiologic practice in retinitis pigmentosa: from phenotyping to biobanking;Chizzolini;Curr. Genomics,2011

3. Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa;Collin;Am. J. Hum. Genet.,2010

4. Retinitis pigmentosa;Hartong;Lancet,2006

5. Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13);McKie;Hum. Mol. Genet.,2001

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