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References
1
1.Dhar, R, Reardon, W, McMahon, CJ. Biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiency. Cardiol Young2014; 15: 1–3.Google Scholar
2
2.Finsterer, J, Stöllberger, C, Blazek, G, Sehnal, E. Familal left ventricular hypertrabeculation (noncompaction) is myopathic. Int J Cardiol2013; 164: 312–317.CrossRefGoogle ScholarPubMed
3
3.Correia, E, Rodrigues, B, Santos, L, et al. Noncompaction of the ventricular myocardium: characterization and follow-up of an affected population. Rev Port Cardiol2011; 30: 323–331.Google ScholarPubMed
4
4.Kirby, DM, Crawford, M, Cleary, MA, Dahl, HH, Dennett, X, Thorburn, DR. Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder. Neurology1999; 52: 1255–1264.CrossRefGoogle ScholarPubMed
5
5.Scaglia, F, Towbin, JA, Craigen, WJ, et al. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. Pediatrics2004; 114: 925–931.CrossRefGoogle ScholarPubMed
6
6.Zarrouk Mahjoub, S, Mehri, S, Ourda, F, et al. Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction. Cardiology2011; 118: 153–158.CrossRefGoogle ScholarPubMed