Mitochondrial disease in adults: recent advances and future promise

Mitochondrial diseases are some of the most common inherited neurometabolic disorders, and major progress has been made in our understanding, diagnosis, and treatment of these conditions in the past 5 years. Development of national mitochondrial disease cohorts and international collaborations has c...

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Veröffentlicht in:	Lancet neurology 2021-07, Vol.20 (7), p.573-584
Hauptverfasser:	Ng, Yi Shiau, Bindoff, Laurence A, Gorman, Gráinne S, Klopstock, Thomas, Kornblum, Cornelia, Mancuso, Michelangelo, McFarland, Robert, Sue, Carolyn M, Suomalainen, Anu, Taylor, Robert W, Thorburn, David R, Turnbull, Doug M
Format:	Artikel
Sprache:	eng
Schlagworte:	Ataxia Atrophy Congenital diseases Convulsions & seizures Disease Disease transmission Dysphagia Epilepsy Family medical history Gene therapy Genes Hearing loss Medical treatment Metabolic disorders Metabolism Mitochondrial DNA Next-generation sequencing Peripheral neuropathy Phenotypes Reproductive technologies Spectrum analysis Stroke
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