Work

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Year: 2001

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/323156

Authors: Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia, Tama Sobe, Fabian Glaser, Raquel Rabionet, Maria Lourdes Arbones, Angelo Notarangelo, Enzo Di Iorio, Massimo Carella, Leopoldo Zelante, Xavier Estivill, Karen B. Avraham, Paolo Gasparini

Institutions: Casa Sollievo della Sofferenza, Tel Aviv University, Duran i Reynals Hospital, Telethon Institute Of Genetics And Medicine

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funder: Fogarty International Center

Awards: G3694000722, GENETICS OF HEARING LOSS IN ISRAELI KINDREDS

OpenAlex ID: W1974866093

FWCI: 6.784

Cites: 21

Cited by: 243

Related to: 10