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| 1. | Title: Hereditary optic atrophies
Author(s): Poloschek CM, Lagreze WA Source: OPHTHALMOLOGE Volume: 106 Issue: 9 Pages: 845-856 Published: SEP 2009 |
| 2. | Title: Inherited mitochondrial optic neuropathies
Author(s): Yu-Wai-Man P, Griffiths PG, Hudson G, et al. Source: JOURNAL OF MEDICAL GENETICS Volume: 46 Issue: 3 Pages: 145-158 Published: MAR 2009 |
| 3. | Title: Mitochondrial DNA Haplogroups M7b1 ' 2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G -> A Mutation
Author(s): Ji YL, Zhang AM, Jia XY, et al. Source: AMERICAN JOURNAL OF HUMAN GENETICS Volume: 83 Issue: 6 Pages: 760-768 Published: DEC 12 2008 |
| 4. | Title: Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background
Author(s): Hudson G, Carelli V, Spruijt L, et al. Source: AMERICAN JOURNAL OF HUMAN GENETICS Volume: 81 Issue: 2 Pages: 228-233 Published: AUG 2007 |
| 5. | Title: Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy
Author(s): Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, et al. Source: JOURNAL OF HUMAN GENETICS Volume: 51 Issue: 12 Pages: 1110-1117 Published: 2006 |
| 6. | Title: Mitochondrial abnormalities in patients with LHON-like optic neuropathies
Author(s): Abu-Amero KK, Bosley TM Source: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE Volume: 47 Issue: 10 Pages: 4211-4220 Published: OCT 2006 |
| 7. | Title: Leber's hereditary optic neuropathy: A multifactorial disease
Author(s): Yen MY, Wang AG, Wei YH Source: PROGRESS IN RETINAL AND EYE RESEARCH Volume: 25 Issue: 4 Pages: 381-396 Published: JUL 2006 |
| 8. | Title: The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees
Author(s): Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, et al. Source: JOURNAL OF HUMAN GENETICS Volume: 51 Issue: 4 Pages: 298-304 Published: 2006 |
| 9. | Title: De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathology
Author(s): Zhadanov SI, Atamanov VV, Zhadanov NI, et al. Source: JOURNAL OF HUMAN GENETICS Volume: 51 Issue: 3 Pages: 161-170 Published: 2006 |
| 10. | Title: Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study
Author(s): Quiros PA, Torres RJ, Salomao S, et al. Source: BRITISH JOURNAL OF OPHTHALMOLOGY Volume: 90 Issue: 2 Pages: 150-153 Published: FEB 2006 |