Summary: Am. J. Hum. Genet. 69:635­640, 2001
635
Report
MYO6, the Human Homologue of the Gene Responsible for Deafness in
Snell's Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic
Hearing Loss
Salvatore Melchionda,1,*
Nadav Ahituv,2,*
Luigi Bisceglia,1
Tama Sobe,2
Fabian Glaser,3
Raquel Rabionet,4
Maria Lourdes Arbones,4
Angelo Notarangelo,1
Enzo Di Iorio,5
Massimo Carella,5
Leopoldo Zelante,1
Xavier Estivill,4
Karen B. Avraham,2
and Paolo Gasparini1

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

Collections: Biology and Medicine