Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review
Author:
Funder
Fondazione Telethon
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics(clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13023-018-0770-1.pdf
Reference33 articles.
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2. Ciafaloni E, Ricci E, Shanske S, Moraes CT, Silvestri G, Hirano M, Simonetti S, Angelini C, Donati MA, Garcia C, et al. MELAS: clinical features, biochemistry, and molecular genetics. Ann Neurol. 1992;31(4):391–8.
3. Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Mitchell P, Sue CM. Population prevalence of the MELAS A3243G mutation. Mitochondrion. 2007;7(3):230–3. Epub 2007 Jan 8
4. P Z, Wilichowski E. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies. Laryngoscope. 2001;111(3):515–21.
5. Kullar PJ, Quail J, Lindsey P, Ja W, Horvath R, Yu-Wai-Man P, Gorman GS, Taylor RW, Ng Y, McFarland R, Moore BCJ, Chinnery PF. Both mitochondrial DNA and mitonuclear gene mutations can cause hearing loss through cochlear dysfunction. Brain. 2016;139:1–5.e33. https://doi.org/10.1093/brain/aww051 .
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