Human Genome Epidemiology Literature Finder
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Query Trace: Deafness and NEDD4[original query] |
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Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes. BMC medical genomics 2018 Sep 11 (1): 77. Lewis Morag A, Nolan Lisa S, Cadge Barbara A, Matthews Lois J, Schulte Bradley A, Dubno Judy R, Steel Karen P, Dawson Sally |
- Page last reviewed:Feb 1, 2024
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