A new point mutation on exon 2 of parkin gene in Parkinson's disease

被引：0
|
作者：
Xu, Yanming [1 ]
Liu, Zhuolin [1 ]
Wang, Yukai [1 ]
Tao, Enxiang [1 ]
Chen, Guojun [1 ]
Chen, Biao [1 ]
机构：
[1] Department of Neurology, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong 510080, China
来源：
Chinese Journal of Medical Genetics | 2002年 / 19卷 / 05期
关键词：
Polymerase chain reaction (PCR) - Polymorphism;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：409 / 411
相关论文
共 50 条
  • [21] Early-onset Parkinson's disease and the Parkin gene
    Matas, IF
    Alvarez, VM
    Coto, E
    Ribacoba, R
    Guisasola, L
    Salvador, C
    MOVEMENT DISORDERS, 2002, 17 : S33 - S34
  • [22] Gene therapy for Parkinson's disease by rAAV-parkin
    Mochizuki, H
    Yamada, M
    Mizuno, Y
    MOVEMENT DISORDERS, 2004, 19 : S243 - S243
  • [23] PARKIN GENE THERAPY IN A MOUSE MODEL OF PARKINSON'S DISEASE
    Yasuda, Toru
    Nihira, Tomoko
    Hayakawa, Hideki
    Ren, Yong-Ri
    Hattori, Nobutaka
    Mizuno, Yoshikuni
    Mochizuki, Hideki
    JOURNAL OF GENE MEDICINE, 2009, 11 (12): : 1174 - 1174
  • [24] Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease
    Zimprich, A
    Asmus, F
    Leitner, P
    Castro, M
    Bereznai, B
    Homann, N
    Ott, E
    Rutgers, AWF
    Wieditz, G
    Trenkwalder, C
    Gasser, T
    NEUROGENETICS, 2003, 4 (04) : 219 - 220
  • [25] Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson′s disease
    Alexander Zimprich
    Friedrich Asmus
    Petra Leitner
    Mirna Castro
    Benjamin Bereznai
    Nikolaus Homann
    Erwin Ott
    A. Wijnand F. Rutgers
    Gyri Wieditz
    Claudia Trenkwalder
    Thomas Gasser
    Neurogenetics, 2003, 4 : 219 - 220
  • [26] Mutation screening and association analysis of the Parkin gene in Parkinson's disease patients from South West China
    Peng, R
    Gou, Y
    Yuan, Q
    Li, T
    Latsoudis, H
    Collier, DA
    MOVEMENT DISORDERS, 2002, 17 : S65 - S66
  • [27] Parkinson's disease with Lewy bodies associated with a heterozygous PARKIN dosage mutation
    Sharp, Madeleine E.
    Marder, Karen S.
    Cote, Lucien
    Clark, Lorraine N.
    Nichols, William C.
    Vonsattel, Jean-Paul
    Alcalay, Roy N.
    MOVEMENT DISORDERS, 2014, 29 (04) : 566 - 568
  • [28] Parkin mutation may be associated with serious akinesia in a patient with Parkinson's disease
    Uchihara, Yuto
    Kataoka, Hiroshi
    Yoshino, Hiroyo
    Syobatake, Ryogo
    Hattori, Nobutaka
    Ueno, Satoshi
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 379 : 119 - 121
  • [29] Parkin mutation analysis in clinic patients with early onset Parkinson's disease
    Poorkaj, P
    Nutt, J
    Gancher, S
    Bird, T
    Steinbart, E
    Schellenberg, G
    Payami, H
    NEUROLOGY, 2004, 62 (07) : A89 - A89
  • [30] Gene mutation detected in Parkinson's disease
    Passey, S
    LANCET NEUROLOGY, 2005, 4 (03): : 142 - 143
12345