Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging

被引:0
作者
Perry G Ridge
Taylor J Maxwell
Spencer J Foutz
Matthew H Bailey
Christopher D Corcoran
JoAnn T Tschanz
Maria C Norton
Ronald G Munger
Elizabeth O'Brien
Richard A Kerber
Richard M Cawthon
John SK Kauwe
机构
[1] Brigham Young University,Department of Biology
[2] ARUP Institute for Clinical and Experimental Pathology,Human Genetics Center
[3] University of Texas School of Public Health,Department of Mathematics and Statistics
[4] Utah State University,Center for Epidemiologic Studies
[5] Utah State University,Department of Psychology
[6] Utah State University,Department of Family Consumer and Human Development
[7] Utah State University,Department of Nutrition, Dietetics, and Food Sciences
[8] Utah State University,Department of Epidemiology and Population Health
[9] University of Louisville,Department of Human Genetics
[10] University of Utah,undefined
来源
BMC Bioinformatics | / 15卷
关键词
Mitochondrial Genome; Mitochondrial Disease; Missense Variant; Haplotype Network; Mitochondrial Haplogroups;
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[1]  
Sequeira A(2012)Mitochondrial mutations and polymorphisms in psychiatric disorders Frontiers in genetics 3 103-308
[2]  
Martin MV(2004)Molecular evidence for mitochondrial dysfunction in bipolar disorder Archives of general psychiatry 61 300-506
[3]  
Rollins B(1986)Late-onset hereditary myopathy with abnormal mitochondria and progressive dementia Acta neurologica Scandinavica 73 502-20
[4]  
Moon EA(2004)A "mitochondrial cascade hypothesis" for sporadic Alzheimer's disease Med Hypotheses 63 8-315
[5]  
Bunney WE(2009)The Alzheimer's disease mitochondrial cascade hypothesis: an update Exp Neurol 218 308-459
[6]  
Macciardi F(1994)Mitochondrial diabetes revisited Nature genetics 7 458-304
[7]  
Lupoli S(2011)Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy Biochemical and biophysical research communications 415 300-6210
[8]  
Smith EN(1994)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 of the United States of America 91 6206-937
[9]  
Kelsoe J(1990)Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation Cell 61 931-144
[10]  
Magnan CN(2002)Leigh disease associated with a novel mitochondrial DNA ND5 mutation European journal of human genetics : EJHG 10 141-98