A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family.
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J. Sahel | S. Bhattacharya | I. Audo | S. Mohand-Saïd | W. Carpentier | K. Bujakowska | C. Lonjou | C. Zeitz | A. Antonio | A. Germain | Marie‐Elise Lancelot | Sophie Tronche