Application of next-generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss

Interruptions in the activity of mitochondria induced by mutations in the mitochondrial genome (mtDNA) can be the source of numerous diseases including hearing loss (HL). One of the mitochondrial variants responsible for HL is the m.7511T>C mutation located in the mitochondrially encoded tRNA ser...

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Detalles Bibliográficos
Autores principales: Lechowicz, Urszula, Pollak, Agnieszka, Frączak, Agnieszka, Rydzanicz, Małgorzata, Stawiński, Piotr, Lorens, Artur, Skarżyński, Piotr H., Skarżyński, Henryk, Płoski, Rafał, Ołdak, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780123/
https://www.ncbi.nlm.nih.gov/pubmed/29257206
http://dx.doi.org/10.3892/mmr.2017.8064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780123/
https://www.ncbi.nlm.nih.gov/pubmed/29257206
http://dx.doi.org/10.3892/mmr.2017.8064

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