These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
93 related articles for article (PubMed ID: 8457609)
1. PCR amplification using a single cell allows the detection of the mtDNA lesion associated with Leber's hereditary optic neuropathy. Erickson CE; Castora FJ Biochim Biophys Acta; 1993 Mar; 1181(1):77-82. PubMed ID: 8457609 [TBL] [Abstract][Full Text] [Related]
2. Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy. Kormann BA; Schuster H; Berninger TA; Leo-Kottler B Hum Genet; 1991 Nov; 88(1):98-100. PubMed ID: 1959931 [TBL] [Abstract][Full Text] [Related]
4. Molecular genetics of Leber's hereditary optic neuropathy: study of a six-generation family from Western Australia. Sudoyo H; Marzuki S; Mastaglia F; Carroll W J Neurol Sci; 1992 Mar; 108(1):7-17. PubMed ID: 1352537 [TBL] [Abstract][Full Text] [Related]
5. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification. Nørby S Hum Mutat; 1993; 2(4):309-13. PubMed ID: 8401538 [TBL] [Abstract][Full Text] [Related]
6. [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 [TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction. Wallace DC; Lott MT; Lezza AM; Seibel P; Voljavec AS; Shoffner JM Pediatr Res; 1990 Nov; 28(5):525-8. PubMed ID: 2123980 [TBL] [Abstract][Full Text] [Related]
9. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249 [TBL] [Abstract][Full Text] [Related]
10. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy. Isashiki Y; Nakagawa M Jpn J Ophthalmol; 1991; 35(3):259-67. PubMed ID: 1770665 [TBL] [Abstract][Full Text] [Related]
11. Variable genotype of Leber's hereditary optic neuropathy patients. Lott MT; Voljavec AS; Wallace DC Am J Ophthalmol; 1990 Jun; 109(6):625-31. PubMed ID: 2346190 [TBL] [Abstract][Full Text] [Related]
12. [A molecular genetic study of Leber's disease]. Zhang LS Zhonghua Yan Ke Za Zhi; 1993 Mar; 29(2):103-4. PubMed ID: 8404350 [TBL] [Abstract][Full Text] [Related]
13. Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism. Mashima Y; Saga M; Hiida Y; Oguchi Y; Wakakura M; Kudoh J; Shimizu N Invest Ophthalmol Vis Sci; 1995 Jul; 36(8):1714-20. PubMed ID: 7601652 [TBL] [Abstract][Full Text] [Related]
14. Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming. Nørby S; Lestienne P; Nelson I; Rosenberg T Biochem Biophys Res Commun; 1991 Mar; 175(2):631-6. PubMed ID: 2018507 [TBL] [Abstract][Full Text] [Related]
15. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy. Yen MY; Yen TC; Pang CY; Liu JH; Wei YH Invest Ophthalmol Vis Sci; 1992 Jul; 33(8):2561-6. PubMed ID: 1634353 [TBL] [Abstract][Full Text] [Related]
16. Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. Holt IJ; Miller DH; Harding AE J Med Genet; 1989 Dec; 26(12):739-43. PubMed ID: 2575667 [TBL] [Abstract][Full Text] [Related]
17. DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens. Mashima Y; Hiida Y; Kubota R; Oguchi Y; Kudoh J; Shimizu N Am J Ophthalmol; 1993 Dec; 116(6):773-4. PubMed ID: 8250088 [No Abstract] [Full Text] [Related]
18. Mutation-specific PCR: a rapid and inexpensive diagnostic method, as exemplified by mitochondrial DNA analysis in Leber's hereditary optic neuropathy. Nørby S DNA Cell Biol; 1993; 12(6):549-52. PubMed ID: 8101084 [TBL] [Abstract][Full Text] [Related]
20. A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations. Hwang JM Korean J Ophthalmol; 2000 Jun; 14(1):45-8. PubMed ID: 10933019 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]