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.
9. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation. Yamada K, Mashima Y, Kigasawa K, Miyashita K, Wakakura M, Oguchi Y. J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781 [Abstract] [Full Text] [Related]
12. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation. Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T. Eur J Paediatr Neurol; 2002 Jun; 6(2):121-3. PubMed ID: 11995959 [Abstract] [Full Text] [Related]
13. [Correlation between clinical and molecular genetic findings in Leber's optic atrophy]. Leo-Kottler B, Christ-Adler M, Reck B, Wissinger B, Zrenner E. Ophthalmologe; 1995 Feb; 92(1):86-92. PubMed ID: 7719084 [Abstract] [Full Text] [Related]