Human Genome Epidemiology Literature Finder
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Query Trace: Epilepsy and FOXI1[original query] |
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Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts. BMC medical genetics 2013 14 85. Landa Priya, Differ Ann-Marie, Rajput Kaukab, Jenkins Lucy, Bitner-Glindzicz Mar |
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- Page last updated:Apr 22, 2024
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