Hemi dystonia from a mitochondrial mutation in MT-ND6
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Abstract
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Jordanian American Physician Academy
Reference6 articles.
1. References:
2. Jun AS, Brown MD, Wallace DC. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia. Proceedings of the National Academy of Sciences. 1994;91(13):6206-6210. doi:10.1073/pnas.91.13.6206
3. Shoffner JM, Brown MD, Stugard C, et al. Leber’s hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation. Ann Neurol. 1995;38(2):163-169. doi:10.1002/ana.410380207
4. Watanabe M, Mita S, Takita T, Goto Y, Uchino M, Imamura S. Leber’s hereditary optic neuropathy with dystonia in a Japanese family. J Neurol Sci. 2006;243(1-2):31-34. doi:10.1016/j.jns.2005.11.003
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