Mitochondrial mutations in maternally inherited hearing loss

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.3243...

Descripción completa

Detalles Bibliográficos
Autores principales: Mutai, Hideki, Watabe, Takahisa, Kosaki, Kenjiro, Ogawa, Kaoru, Matsunaga, Tatsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359870/
https://www.ncbi.nlm.nih.gov/pubmed/28320335
http://dx.doi.org/10.1186/s12881-017-0389-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359870/
https://www.ncbi.nlm.nih.gov/pubmed/28320335
http://dx.doi.org/10.1186/s12881-017-0389-4

Ejemplares similares