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Paper Details

A novel variant in <i>DMXL2</i> gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.
Exp Biol Med (Maywood)
6
2021
Author NameAffiliation
Abdul NasirAjou University
Suzanne M LealCenter for Statistical Genetics, Taub Institute for Alzheimer's Disease and the Aging Brain, Columbia University Medical Centre
Ambroise WonkamUniversity of Cape Town
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Datasets

Release 1.2