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Amedeo Smart

Independent Medical Education


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Velde HM, Homans NC, Goedegebure A, Lanting CP, et al. Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands. J Med Genet 2023 May 10:jmg-2023-109146. doi: 10.1136/jmg-2023-109146.
PMID: 37164627


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