Multiple Mutations ofMYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss-Reference-Cited by-同舟云学术

Multiple Mutations ofMYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

Published:2003-06 Issue:6 Volume:72 Page:1571-1577
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Donaudy Francesca,Ferrara Antonella,Esposito Laura,Hertzano Ronna,Ben-David Orit,Bell Rachel E.,Melchionda Salvatore,Zelante Leopoldo,Avraham Karen B.,Gasparini Paolo

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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3. A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13–q14 in a large Italian family;D’Adamo;Hum Genet,2003

4. Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia;Dumont;J Assoc Res Otolaryngol,2002

5. Unconventional myosins and the genetics of hearing loss;Friedman;Am J Med Genet,1999

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