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26. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis. Kim JY; Hwang JM; Park SS Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111 [TBL] [Abstract][Full Text] [Related]
27. [Observations on several cases of Leber's disease]. Gerhard JP; Flament J; Franck H; Mack G Bull Soc Ophtalmol Fr; 1971; 71(5-6):607-15. PubMed ID: 5317155 [No Abstract] [Full Text] [Related]
35. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation. Shoffner JM; Brown MD; Stugard C; Jun AS; Pollock S; Haas RH; Kaufman A; Koontz D; Kim Y; Graham JR Ann Neurol; 1995 Aug; 38(2):163-9. PubMed ID: 7654063 [TBL] [Abstract][Full Text] [Related]
36. [Neurologic and mental disorders in carriers of Leber's disease]. Bieder J; Nourry C; Durieux S Ann Med Psychol (Paris); 1982 Mar; 140(3):360-9. PubMed ID: 7137761 [No Abstract] [Full Text] [Related]