Mitochondrial mutations in maternally inherited hearing loss
Mitochondrial mutations in maternally inherited hearing loss
About this item
Full title
Author / Creator
Publisher
England: BioMed Central
Journal title
Language
English
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Publication information
Publisher
England: BioMed Central
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Scope and Contents
Contents
Although the mitochondrial DNA (mtDNA) mutations m.1555A > G and m.3243A > G are the primary causes of maternally inherited sensorineural hearing loss (SNHL), several other mtDNA mutations are also reported to be associated with SNHL.
Screening of m.1555A > G and m.3243A > G mutations was performed for 145 probands. Nine probands fulfilled the f...
Alternative Titles
Full title
Mitochondrial mutations in maternally inherited hearing loss
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5359870
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5359870
Other Identifiers
ISSN
1471-2350
E-ISSN
1471-2350
DOI
10.1186/s12881-017-0389-4
