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9. Cytogenetic damage in peripheral lymphocytes of mitochondrial disease patients. Naccarati A; Molinu S; Mancuso M; Siciliano G; Migliore L Neurol Sci; 2000; 21(5 Suppl):S963-5. PubMed ID: 11382196 [TBL] [Abstract][Full Text] [Related]
10. Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies. Huang CC; Kuo HC; Chu CC; Liou CW; Ma YS; Wei YH J Biomed Sci; 2002; 9(6 Pt 1):527-33. PubMed ID: 12372990 [TBL] [Abstract][Full Text] [Related]
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14. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study. Hammans SR; Sweeney MG; Hanna MG; Brockington M; Morgan-Hughes JA; Harding AE Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089 [TBL] [Abstract][Full Text] [Related]
15. The therapy of respiratory chain encephalomyopathy: a critical review of the past and current perspective. Walker UA; Byrne E Acta Neurol Scand; 1995 Oct; 92(4):273-80. PubMed ID: 8848932 [TBL] [Abstract][Full Text] [Related]
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17. [Mitochondrial encephalomyopathies: 3243 mutation as a central matter]. Goto Y; Nonaka I Rinsho Shinkeigaku; 1995 Dec; 35(12):1425-6. PubMed ID: 8752418 [TBL] [Abstract][Full Text] [Related]