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Academic Journal

De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment

Subjects: Adult; Male; Heterozygote

  • Source: Hum GenetSmits, J J, Oostrik, J, Beynon, A J, Kant, S G, de Koning Gans, P A M, Rotteveel, L J C, Klein Wassink-Ruiter, J S, Free, R H, Maas, S M, van de Kamp, J, Merkus, P, Koole, W, Feenstra,

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  • 1-10 of  28 results for ""retrocochlear pathology""