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DOI: 10.1086/323156
¤ OpenAccess: Hybrid
This work has “Hybrid” OA status. This means it is free under an open license in a toll-access journal.
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,Nadav Ahituv,Luigi Bisceglia,Tama Sobe,Fabian Glaser,Raquel Rabionet,Mariona Arbonés,Angelo Notarangelo,Enzo Di Iorio,Massimo Carella,Leopoldo Zelante,Xavier Estivill,Karen B. Avraham,Paolo Gasparini
Missense mutation
Genetics
Locus (genetics)
2001
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“MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss” is a paper by Salvatore Melchionda Nadav Ahituv Luigi Bisceglia Tama Sobe Fabian Glaser Raquel Rabionet Mariona Arbonés Angelo Notarangelo Enzo Di Iorio Massimo Carella Leopoldo Zelante Xavier Estivill Karen B. Avraham Paolo Gasparini published in 2001. It has an Open Access status of “hybrid”. You can read and download a PDF Full Text of this paper here.