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6. Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene. Akanuma J; Muraki K; Komaki H; Nonaka I; Goto Y J Hum Genet; 2000; 45(6):337-41. PubMed ID: 11185741 [TBL] [Abstract][Full Text] [Related]
7. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy]. Ito T Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824 [TBL] [Abstract][Full Text] [Related]
8. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies. Filosto M; Mancuso M; Vives-Bauza C; Vilà MR; Shanske S; Hirano M; Andreu AL; DiMauro S Ann Neurol; 2003 Oct; 54(4):524-6. PubMed ID: 14520667 [TBL] [Abstract][Full Text] [Related]
9. A patient with two mitochondrial DNA mutations causing PEO and LHON. Melberg A; Moslemi AR; Palm O; Raininko R; Stålberg E; Oldfors A Eur J Med Genet; 2009; 52(1):47-8. PubMed ID: 19015050 [TBL] [Abstract][Full Text] [Related]
10. [Diseases of mitochondrial DNA]. Montoya J; Playán A; Solano A; Alcaine MJ; López-Pérez MJ; Pérez-Martos A Rev Neurol; 2000 Aug 16-31; 31(4):324-33. PubMed ID: 11008288 [TBL] [Abstract][Full Text] [Related]
11. [Mitochondrial cardiomyopathies: a new entity in cardiology research and diagnosis]. Bernucci P; D'Amati G; Casali C; De Biase L; Autore C; Fedele F; Gallo P G Ital Cardiol; 1996 Sep; 26(9):1031-7. PubMed ID: 9036041 [No Abstract] [Full Text] [Related]
12. [Mitochondrial medicine: human chromosome 25 and mitochondrial diseases]. Walker UA Dtsch Med Wochenschr; 1999 Feb; 124(7):189-92. PubMed ID: 10093578 [No Abstract] [Full Text] [Related]
15. [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; 139(26):1322-6. PubMed ID: 7617049 [No Abstract] [Full Text] [Related]
16. [Chronic progressive external ophthalmoplegia--symptom or syndrome?]. Bau V; Deschauer M; Zierz S Klin Monbl Augenheilkd; 2009 Oct; 226(10):822-8. PubMed ID: 19830638 [TBL] [Abstract][Full Text] [Related]
17. Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome. De Joanna G; Santorelli FM; Casali C; Brescia-Morra V; Perretti A; Santoro L J Hum Genet; 2000; 45(2):109-11. PubMed ID: 10721677 [TBL] [Abstract][Full Text] [Related]