Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

F. Donaudy, L. Zheng, R. Ficarella, E. Ballana, M. Carella, S. Melchionda, X. Estivill, J. R. Bartles, Paolo Gasparini*

*Corresponding author for this work

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Medicine & Life Sciences