Hearing Disorders; Stanford University School of Medicine Describes Findings in Hearing Loss (Exome...
Hearing Disorders; Stanford University School of Medicine Describes Findings in Hearing Loss (Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss)
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Publisher
Atlanta: NewsRx
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Language
English
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Publisher
Atlanta: NewsRx
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Contents
The news correspondents obtained a quote from the research from the Stanford University School of Medicine, "Analysis of three distinct families revealed several candidate loci in two families and a single strong candidate gene, MYH7B, for hearing loss in one family. MYH7B encodes a Type II myosin, consistent with a role for cytoskeletal proteins i...
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Full title
Hearing Disorders; Stanford University School of Medicine Describes Findings in Hearing Loss (Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss)
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TN_cdi_proquest_wirefeeds_1658109207
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_wirefeeds_1658109207
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ISSN
1552-2466
E-ISSN
1552-2474
