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Hearing Is Normal without Connexin30Journal of Neuroscience, 2013, 33 (2), pp.430-434. ⟨10.1523/JNEUROSCI.4240-12.2013⟩
Journal articles
hal-04027322v1
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Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.American Journal of Human Genetics, 2013, 92 (5), pp.707-24. ⟨10.1016/j.ajhg.2013.03.024⟩
Journal articles
inserm-00836181v1
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Exocytotic Machineries of Vestibular Type I and Cochlear Ribbon Synapses Display Similar Intrinsic Otoferlin-Dependent Ca2+ Sensitivity But a Different Coupling to Ca2+ ChannelsJournal of Neuroscience, 2014, 34 (33), pp.10853-10869. ⟨10.1523/JNEUROSCI.0947-14.2014⟩
Journal articles
hal-04160516v1
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Thérapie génique des surdités humainesMédecine/Sciences, 2013, 29 (10), pp.883 - 889. ⟨10.1051/medsci/20132910016⟩
Journal articles
hal-04159599v1
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