Leigh disease associated with a novel mitochondrial DNA ND5 mutation
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Robert W Taylor | Robert W. Taylor | Michael K. Hutchinson | D. Turnbull | Michael Hutchinson | Douglass M Turnbull | Andrew AM Morris | A. Morris | Robert W. Taylor
[1] G. Attardi,et al. Tight Control of Respiration by NADH Dehydrogenase ND5 Subunit Gene Expression in Mouse Mitochondria , 2000, Molecular and Cellular Biology.
[2] S. Dimauro,et al. A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene , 1995, Neuromuscular Disorders.
[3] Robert W. Taylor,et al. Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene , 2001, Annals of neurology.
[4] D. Ellison,et al. A mitochondrial DNA tRNAVal point mutation associated with adult-onset Leigh syndrome , 1997, Neurology.
[5] Peter B. McGarvey,et al. The Protein Information Resource (PIR) , 2000, Nucleic Acids Res..
[6] I. Nelson,et al. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS , 1999, Annals of neurology.
[7] D. Turnbull,et al. Deficiency of respiratory chain complex I is a common cause of leigh disease , 1996, Annals of neurology.
[8] D. Reddihough,et al. Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families , 2000, Annals of neurology.
[9] D. Thorburn,et al. Respiratory chain complex I deficiency , 1999, Neurology.
[10] H. Dahl,et al. Getting to the nucleus of mitochondrial disorders: identification of respiratory chain-enzyme genes causing Leigh syndrome. , 1998, American journal of human genetics.
[11] D. Turnbull,et al. The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations. , 2001, Nucleic acids research.