Summary: Am. J. Hum. Genet. 72:1571­1577, 2003
1571
Report
Multiple Mutations of MYO1A, a Cochlear-Expressed Gene,
in Sensorineural Hearing Loss
Francesca Donaudy,1
Antonella Ferrara,2
Laura Esposito,1
Ronna Hertzano,3
Orit Ben-David,3
Rachel E. Bell,4
Salvatore Melchionda,5
Leopoldo Zelante,5
Karen B. Avraham,3
and Paolo Gasparini1,2
1
Telethon Institute of Genetics and Medicine and 2
Genetica Medica, Dipartimento di Patologia Generale, Seconda Universita` di Napoli,
Naples, Italy; 3
Department of Human Genetics and Molecular Medicine, Sackler School of Medicine, and 4

Source: Avraham, Karen - Department of Human Genetics and Molecular Medicine, Tel Aviv University

Collections: Biology and Medicine