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Yaming Wu

First Affiliated Hospital of Wenzhou Medical University

5

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67

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A study on the system of self-evaluation of the visual acuity based on WeChat platform

2018 Investigative Ophthalmology & Visual Science
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Identification of a rhodopsin gene mutation in a large family with autosomal dominant retinitis pigmentosa

2016 Scientific Reports
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Identification of a Novel GJA8 (Cx50) Point Mutation Causes Human Dominant Congenital Cataracts

2015 Scientific Reports
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Identification of Three Novel Mutations in the FRMD7 Gene for X-linked Idiopathic Congenital Nystagmus

2015 Scientific Reports
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Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing

2014 PLOS ONE
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