Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation-Reference-Cited by-同舟云学术

Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation

Published:1995-08 Issue:2 Volume:38 Page:163-169
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Shoffner John M.,Brown Michael D.,Stugard Carol,June Albert S.,Pollock Stephen,Haas Richard H.,Kaufman Allan,Koontz Deborah,Kim Yoon,Graham Jennifer R.,Smith Edwin,Dixon John,Wallace Douglas C.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference24 articles.

1. A mitochondrial DNA mutation at np 14459 of the ND6 gene associated with maternally inherited Leber's hereditary optic neuropathy and dystonia;Jun;Proc Natl Acad Sci USA,1994

2. Purification of three ironsulfur proteins from the iron-protein fragment of mitochondrial NADH-ubiquinone oxidoreductase;Ragan;Biochemistry,1982

3. Resolution of mitochondrial NADH dehydrogenase and isolation of two ironsulfur proteins;Ragan;Biochemistry,1982

4. Leber's disease and dystonia: a mitochondrial disease;Novotny;Neurology,1986

5. Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease;Wallace;Cell,1988

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