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Bing Dong

Capital Medical University

12

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227

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Comprehensive screening of CYP4V2 in a cohort of Chinese patients with Bietti crystalline dystrophy

2018 Molecular Vision
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Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations.

2016 Investigative Ophthalmology & Visual Science
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Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis

2014 Molecular Vision
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A novel GUCY2D mutation in a Chinese family with dominant cone dystrophy.

2013 Molecular Vision
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Two novel PRPF31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa

2013 Molecular Vision
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Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II

2011 Molecular Vision
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Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II

2008 Molecular Vision
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Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1.

2008 Molecular Vision
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Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy.

2008 Molecular Vision
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Identification of a novel VEGFR-3 missense mutation in a Chinese family with hereditary lymphedema type I.

2007 Journal of Genetics and Genomics
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Citations (9)