Christine Petit
0000-0002-9069-002X
5 papers found
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Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies
Central auditory deficits associated with genetic forms of peripheral deafness
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis
A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in USH1C That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss
Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses
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