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Prevalence and nature of connexin 26 mutations in children with non‐syndromic deafness

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Year: 2001
Type: article
Study design: Observational Study
Source: The Medical Journal of Australia
DOI: 10.5694/j.1326-5377.2001.tb143093.x
Authors: Hans‐Henrik M Dahl, Kerryn Saunders, Therese M Kelly, Amelia H Osborn, Stephen Wilcox, Barbara Cone‐Wesson, Julia L Wunderlich, Desiree Du Sart, Maria Kamarinos, Robert J McKinlay Gardner, Shirley Dennehy, Robert Williamson, Neil Vallance, Patricia Mutton
Institutions: Royal Children's Hospital, The University of Melbourne, Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Monash University, Children's Hospital at Westmead, Westmead Hospital
Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2233570700
FWCI: 1.766
Cites: 21
Cited by: 43
Related to: 10
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