Posts

Journal Club: Carboxypeptidase D (CPD) gene variants as the cause of familial, recessive hearing loss

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Journal Club: Loss of OSBPL2 lead to impairment of the barrier function of the small blood vessels: implication for DFNA hearing loss caused by OSBPL2 variants.

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Journal Club: Structural analysis of P2X2 receptors show 2 different desensitization confirmations

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Journal Club: TRIM71, a gene linked to hydrocephalus, is also linked to some hearing loss via altered development.

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