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2. Noncompaction cardiomyopathy in a neonate presenting with hydrops fetalis and pulmonary hypertension. Rungan S; Wright J Pediatr Cardiol; 2013; 34(8):2003-5. PubMed ID: 23052678 [TBL] [Abstract][Full Text] [Related]
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8. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin. Boustany RN; Aprille JR; Halperin J; Levy H; DeLong GR Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875 [TBL] [Abstract][Full Text] [Related]
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11. A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: A case report with clinical and molecular review. Galvão de Oliveira M; Tengan C; Micheletti C; Ramos de Macedo P; Soares Pinho Cernach MC; Cavole TR; de França Basto M; Filho JS; Virmond LA; Milanezi F; Nakano V; Falconi A; Perrone E Eur J Med Genet; 2021 May; 64(5):104195. PubMed ID: 33746038 [TBL] [Abstract][Full Text] [Related]
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14. Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency. Horvath R; Lochmüller H; Stucka R; Yao J; Shoubridge EA; Kim SH; Gerbitz KD; Jaksch M Biochem Biophys Res Commun; 2000 Sep; 276(2):530-3. PubMed ID: 11027508 [TBL] [Abstract][Full Text] [Related]
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