A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family

International audience

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

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Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

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Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction

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