RIT2, a susceptibility gene for Parkinson's disease in Iranian population

被引:19
作者
Emamalizadeh, Babak [1 ]
Movafagh, Abolfazl [1 ]
Akbari, Mojdeh [1 ]
Kazeminasab, Somayyeh [2 ]
Fazeli, Atena [1 ]
Motallebi, Marzieh [1 ]
Shahidi, Gholam-Ali [3 ]
Petramfar, Peyman [4 ]
Mirfakhraie, Reza [1 ]
Darvish, Hossein [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran
[2] Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran, Iran
[3] Iran Univ Med Sci, Hazrat Rassol Hosp, Movement Disorders Clin, Tehran, Iran
[4] Shiraz Univ Med Sci, Dept Neurol, Shiraz, Iran
关键词
REGION;
D O I
10.1016/j.neurobiolaging.2014.07.013
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
引用
收藏
页码:E27 / E28
页数:2
相关论文
共 9 条
[1]   Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients [J].
Darvish, Hossein ;
Movafagh, Abolfazl ;
Omrani, Mir Davood ;
Firouzabadi, Saghar Ghasemi ;
Azargashb, Eznollah ;
Jamshidi, Javad ;
Khaligh, Ali ;
Haghnejad, Leyla ;
Naeini, Nilofar Safavi ;
Talebi, Atefeh ;
Heidari-Rostami, Hamid Reza ;
Noorollahi-Moghaddam, Hamid ;
Karkheiran, Siamak ;
Shahidi, Gholam-Ali ;
Paknejad, Seyed Mohammad Hassan ;
Ashrafian, Hossein ;
Abdi, Siamak ;
Kayyal, Matin ;
Akbari, Mojdeh ;
Pedram, Negar ;
Emamalizadeh, Babak .
NEUROSCIENCE LETTERS, 2013, 551 :75-78
[2]   Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease [J].
Edwards, Todd L. ;
Scott, William K. ;
Almonte, Cherylyn ;
Burt, Amber ;
Powell, Eric H. ;
Beecham, Gary W. ;
Wang, Liyong ;
Zuchner, Stephan ;
Konidari, Ioanna ;
Wang, Gaofeng ;
Singer, Carlos ;
Nahab, Fatta ;
Scott, Burton ;
Stajich, Jeffrey M. ;
Pericak-Vance, Margaret ;
Haines, Jonathan ;
Vance, Jeffery M. ;
Martin, Eden R. .
ANNALS OF HUMAN GENETICS, 2010, 74 :97-109
[3]   Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease [J].
Hamza, Taye H. ;
Zabetian, Cyrus P. ;
Tenesa, Albert ;
Laederach, Alain ;
Montimurro, Jennifer ;
Yearout, Dora ;
Kay, Denise M. ;
Doheny, Kimberly F. ;
Paschall, Justin ;
Pugh, Elizabeth ;
Kusel, Victoria I. ;
Collura, Randall ;
Roberts, John ;
Griffith, Alida ;
Samii, Ali ;
Scott, William K. ;
Nutt, John ;
Factor, Stewart A. ;
Payami, Haydeh .
NATURE GENETICS, 2010, 42 (09) :781-U75
[4]   Variable phenotypic expression in families with early-onset Parkinsonism due to PRKN mutations [J].
Karkheiran, Siamak ;
Krebs, Catharine E. ;
Darvish, Hossein ;
Asadian, Mojgan ;
Shahidi, Gholam Ali ;
Paisan-Ruiz, Coro .
JOURNAL OF NEUROLOGY, 2014, 261 (06) :1223-1226
[5]   The Sac1 Domain of SYNJ1 Identified Mutated in a Family with Early-Onset Progressive Parkinsonism with Generalized Seizures [J].
Krebs, Catharine E. ;
Karkheiran, Siamak ;
Powell, James C. ;
Cao, Mian ;
Makarov, Vladimir ;
Darvish, Hossein ;
Di Paolo, Gilbert ;
Walker, Ruth H. ;
Shahidi, Gholam Ali ;
Buxbaum, Joseph D. ;
De Camilli, Pietro ;
Yue, Zhenyu ;
Paisan-Ruiz, Coro .
HUMAN MUTATION, 2013, 34 (09) :1200-1207
[6]  
Lin CH, 2013, NEUROBIOL AGING, V34
[7]  
Nielsen SS, 2013, INT J MOL EPIDEMIOL, V4, P61
[8]   Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2 [J].
Pankratz, Nathan ;
Beecham, Gary W. ;
DeStefano, Anita L. ;
Dawson, Ted M. ;
Doheny, Kimberly F. ;
Factor, Stewart A. ;
Hamza, Taye H. ;
Hung, Albert Y. ;
Hyman, Bradley T. ;
Ivinson, Adrian J. ;
Krainc, Dmitri ;
Latourelle, Jeanne C. ;
Clark, Lorraine N. ;
Marder, Karen ;
Martin, Eden R. ;
Mayeux, Richard ;
Ross, Owen A. ;
Scherzer, Clemens R. ;
Simon, David K. ;
Tanner, Caroline ;
Vance, Jeffery M. ;
Wszolek, Zbigniew K. ;
Zabetian, Cyrus P. ;
Myers, Richard H. ;
Payami, Haydeh ;
Scott, William K. ;
Foroud, Tatiana .
ANNALS OF NEUROLOGY, 2012, 71 (03) :370-384
[9]  
Zhang L, 2013, MOL VIS, V19, P1371