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Vanita Berry

UCL Institute of Ophthalmology

6

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26

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Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract.

2020 Genes
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A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract

2018 Ophthalmic Genetics
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A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family

2017 Eye
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