No evidence of an association between the mtDNA 16184-93 polyC tract and late onset dementia

被引:3
作者
Keers, SM [1 ]
Gibson, AM [1 ]
Turnbull, DM [1 ]
Chinnery, PF [1 ]
机构
[1] Med Sch Newcastle Upon Tyne, Dept Neurol, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
D O I
10.1136/jmg.2004.022467
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:957 / 958
页数:2
相关论文
共 7 条
[1]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[2]   Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA [J].
Andrews, RM ;
Kubacka, I ;
Chinnery, PF ;
Lightowlers, RN ;
Turnbull, DM ;
Howell, N .
NATURE GENETICS, 1999, 23 (02) :147-147
[3]   No evidence of an association between the T16189C mtDNA variant and late onset dementia [J].
Gibson, AM ;
Edwardson, JA ;
Turnbull, DM ;
McKeith, IG ;
Morris, CM ;
Chinnery, PF .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (01)
[4]   Persistent heteroplasmy of a mutation in the human mtDNA control region: Hypermutation as an apparent consequence of simple-repeat expansion/contraction [J].
Howell, N ;
Smejkal, CB .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (05) :1589-1598
[5]   A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations [J].
Khogali, SS ;
Mayosi, BM ;
Beattie, JM ;
McKenna, WJ ;
Watkins, H ;
Poulton, J .
LANCET, 2001, 357 (9264) :1265-1267
[6]   The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading [J].
Livesey, KJ ;
Wimhurst, VLC ;
Carter, K ;
Worwood, M ;
Cadet, E ;
Rochette, J ;
Roberts, AG ;
Pointon, JJ ;
Merryweather-Clarke, AT ;
Bassett, ML ;
Jouanolle, AM ;
Mosser, A ;
David, V ;
Poulton, J ;
Robson, KJH .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (01) :6-10
[7]   The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations [J].
Taylor, RW ;
Taylor, GA ;
Durham, SE ;
Turnbull, DM .
NUCLEIC ACIDS RESEARCH, 2001, 29 (15) :art. no.-e74