Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy-Reference-Cited by-同舟云学术

Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy

Published:2016-05 Issue: Volume:146 Page:154-162
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Yin Xiaobei,Yang Liping,Chen Ningning,Cui Hui,Zhao Lin,Feng Lina,Li Aijun,Zhang Huirong,Ma Zhizhong,Li Genlin

Funder

Peking University

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference28 articles.

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2. Bietti's corneal-retinal dystrophy. A 16-year progression;Bernauer;Retina,1992

3. Ueber familiaeres vorkommen von 'retinitis punctata albescens' (verbunden mit 'dystrophia marginalis cristallinea corneae'), glitzern des glaskoerpers und anderen degenerativen augenveraenderungen;Bietti;Klin. Monatsbl. Augenheilkd,1937

4. Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases;Chen;Investig. Ophthalmol. Vis. Sci.,2013

5. Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy;Halford;Ophthalmology,2014

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