论文信息 - Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation - 字舞流文

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

X. Estivill | P. Gasparini | M. Carella | R. Ficarella | E. Ballana | S. Melchionda | F. Donaudy | J. Bartles | Lili Zheng | L. Zheng | Paolo Gasparini | Francesca Donaudy | Xavier Estivill | Massimo Carella | Ester Ballana