Human Genome Epidemiology Literature Finder
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Query Trace: Hearing and VTN[original query] |
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Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon. Human molecular genetics 2020 Oct . Wonkam Ambroise, Manyisa Noluthando, Bope Christian D, Dandara Collet, Chimusa Emile |
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- Page last updated:Apr 22, 2024
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