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5. Update in molecular genetics: mitochondrial energy transduction disorders. Marzuki S, Sudoyo H, Lertrit P. Southeast Asian J Trop Med Public Health; 1995 Dec; 26 Suppl 1():155-61. PubMed ID: 8629096 [No Abstract] [Full Text] [Related]
6. The molecular genetics of mitochondrial cytopathies: the Melbourne experience. Thyagarajan D, Byrne E, Dennet X, Marzuki S. Clin Exp Neurol; 1992 Dec; 29():172-81. PubMed ID: 1343860 [Abstract] [Full Text] [Related]
7. [Diseases caused by mitochondrial DNA mutations]. Wijburg FA, van den Bogert C, de Visser M, Oostra RJ, Bakker PA, Bolhuis PA. Ned Tijdschr Geneeskd; 1995 Jul 01; 139(26):1322-6. PubMed ID: 7617049 [No Abstract] [Full Text] [Related]
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9. Maternal inheritance and the evaluation of oxidative phosphorylation diseases. Shoffner JM. Lancet; 1996 Nov 09; 348(9037):1283-8. PubMed ID: 8909383 [Abstract] [Full Text] [Related]
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18. Abnormal excretion of urinary phospholipids and sulfatide in patients with mitochondrial encephalomyopathies. Uyama E, Kutsukake Y, Hara A, Uemura K, Uchino M, Mita S, Ando M, Taketomi T. Biochem Biophys Res Commun; 1993 Jul 15; 194(1):266-73. PubMed ID: 8333841 [Abstract] [Full Text] [Related]
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