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156 related items for PubMed ID: 2346203
21. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China]. Zhang LS, Huang Y, Li FY. Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643 [Abstract] [Full Text] [Related]
27. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Newman NJ, Lott MT, Wallace DC. Am J Ophthalmol; 1991 Jun 15; 111(6):750-62. PubMed ID: 2039048 [Abstract] [Full Text] [Related]
38. Leber's hereditary optic neuropathy as a cause of severe visual loss in childhood. Moorman CM, Elston JS, Matthews P. Pediatrics; 1993 May 15; 91(5):988-9. PubMed ID: 8474822 [No Abstract] [Full Text] [Related]
39. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON. Rödel G, Laubhan R, Scheuerle A, Skowronek P, Haferkamp O. Eur J Med Res; 1996 Jul 25; 1(10):491-4. PubMed ID: 9438147 [Abstract] [Full Text] [Related]