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Article

Mitochondrial mutations in maternally inherited hearing loss.

BMC medical genetics - 20 Mar 2017

Mutai Hideki, Watabe Takahisa, Kosaki Kenjiro, Ogawa Kaoru, Matsunaga Tatsuo

Abstract excerpt

BACKGROUND: 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. METHODS: Screening of m.1555A > G and m.3243A > G mutations was performed for 145 probands. Nine probands fulfilled the following criteria: 1) bilateral and symmetric...

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Share to Hearing Loss, Sensorineural

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Sequence Analysis, DNA

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Source

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Identifiers

PMID: 28320335
DOI: 10.1186/s12881-017-0389-4
PMCID: PMC5359870

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