Human Genome Epidemiology Literature Finder
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Query Trace: Abnormalities and ESPN[original query] |
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Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation. Journal of medical genetics 2006 Feb 43 (2): 157-61. Donaudy F, Zheng L, Ficarella R, Ballana E, Carella M, Melchionda S, Estivill X, Bartles J R, Gasparini |
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