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Ananya Samanta

University of Mainz

6

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49

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Ataluren for the Treatment of Usher Syndrome 2A Caused by Nonsense Mutations.

2019 International Journal of Molecular Sciences
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Ataluren-mediated read-through of a nonsense mutation in FAM161A gene which causes retinitis pigmentosa

2018 Investigative Ophthalmology & Visual Science
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Das Überlesen von Nonsense-Mutationen

2017 Medizinische Genetik
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Small molecules for targeting nonsense mutations causing ciliopathies

2016 Investigative Ophthalmology & Visual Science
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The SANS-USH2a-whirlin ternary complex of Usher syndrome type 1 and type 2 proteins is disrupted by pathogenic mutations

2015 Investigative Ophthalmology & Visual Science
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