2018•Journal of Human GeneticsRequires access

Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans

Alex Marcel Moreira Dias, Karina Lezirovitz, Fernanda Stávale Nicastro, Beatriz de Castro Andrade Mendes, Regina Célia Mingroni‐Netto

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Key concepts: Hearing loss, Loss function, Genetics, Gene, Biology, Congenital hearing loss, Mutation, Phenotype

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Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans — Research Paper | ScholarLens