Author:
Varhaug Kristin N.,Hikmat Omar,Bindoff Laurence A.
Publisher
Norwegian Medical Association
Reference15 articles.
1. Gorman GS, Schaefer AM, Ng Y et al. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. Ann Neurol 2015; 77: 753–9. [PubMed][CrossRef]
2. Majamaa-Voltti K, Turkka J, Kortelainen ML et al. Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA. J Neurol Neurosurg Psychiatry 2008; 79: 209–11. [PubMed][CrossRef]
3. Majamaa-Voltti KA, Winqvist S, Remes AM et al. A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA. Neurology 2006; 66: 1470–5. [PubMed][CrossRef]
4. Bates MG, Hollingsworth KG, Newman JH et al. Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers. Eur Heart J Cardiovasc Imaging 2013; 14: 650–8. [PubMed][CrossRef]
5. de Laat P, Zweers HE, Knuijt S et al. Dysphagia, malnutrition and gastrointestinal problems in patients with mitochondrial disease caused by the m3243A>G mutation. Neth J Med 2015; 73: 30–6. [PubMed]