TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder i...
TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad
About this item
Full title
Author / Creator
Publisher
United States: John Wiley & Sons, Inc
Journal title
Language
English
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Publication information
Publisher
United States: John Wiley & Sons, Inc
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More information
Scope and Contents
Contents
Background
Sensorineural hearing loss (SNHL) is a common form of hearing loss that can be inherited or triggered by environmental insults; auditory neuropathy spectrum disorder (ANSD) is a SNHL subtype with unique diagnostic criteria. The genetic factors associated with these impairments are vast and diverse, but causal genetic factors are rarel...
Alternative Titles
Full title
TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6081214
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6081214
Other Identifiers
ISSN
2324-9269
E-ISSN
2324-9269
DOI
10.1002/mgg3.397
