Expression and localization of CERKL in the mammalian retina, its response to light-stress, and relationship with NeuroD1 gene-Reference-Cited by-同舟云学术

Expression and localization of CERKL in the mammalian retina, its response to light-stress, and relationship with NeuroD1 gene

Published:2013-01 Issue: Volume:106 Page:24-33
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Mandal Nawajes A.,Tran Julie-Thu A.,Saadi Anisse,Rahman Abul K.,Huynh Tuan-Phat,Klein William H.,Cho Jang-Hyeon

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference38 articles.

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3. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews;Auslender;Investigative Ophthalmology & Visual Science,2007

4. CERKL mutations and associated phenotypes in seven Spanish families with autosomal recessive retinitis pigmentosa;Avila-Fernandez;Investigative Ophthalmology & Visual Science,2008

5. A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33;Bayes;Journal of Medical Genetics,1998

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