Human Genome Epidemiology Literature Finder
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Query Trace: Attention and STRC[original query] |
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DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. Clinical genetics 2015 87 (1): 49-55. Vona B, Hofrichter M A H, Neuner C, Schröder J, Gehrig A, Hennermann J B, Kraus F, Shehata-Dieler W, Klopocki E, Nanda I, Haaf |
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- Page last updated:Apr 22, 2024
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