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authFullName_s : Ieva Sliesoraityte
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An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet , Zied Riahi , Sandra Chantot-Bastaraud , Luce Smagghe , Mélanie Letexier , et al.
European Journal of Human Genetics, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩
Journal articles pasteur-03215026v1

Usher Syndrome and Color Vision

Anne Kurtenbach , Gesa Hahn , Christoph Kernstock , Stephanie Hipp , Ditta Zobor , et al.
Current Eye Research, 2018, 43 (10), pp.1295-1301. ⟨10.1080/02713683.2018.1501804⟩
Journal articles pasteur-03219639v1