Author:
Brown Michael D.,Hosseini Seyed,Steiner Israel,Wallace Douglas C.,Korn-Lubetzki Isabelle
Subject
Clinical Neurology,Neurology
Reference10 articles.
1. 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;Jun;Proc Natl Acad Sci USA,1994
2. Leber's hereditary optic atrophy plus dystonia is caused by a mitochondrial DNA point mutation;Shoffner;Ann Neurol,1995
3. Leber's disease and dystonia: a mitochondrial disease;Novotny;Neurology,1986
4. Clinical spectrum of Leber's hereditary optic neuropathy;Kerrison;Clin Neurosci,1997
5. Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia;De Vries;Am J Hum Genet,1996
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献