Mutation analysis of the PINK1 gene in 642 patients with Parkinson disease

被引:0
|
作者
Kumazawa, Ryuya
Tomiyama, Hiroyuki
Funayama, Manabu
Yoshino, Hiroyo
Takahashi, Hirohide
Yoshii, Fumihito
Mizuno, Yoshikuni
Hattori, Nobutaka
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:S72 / S72
页数:1
相关论文
共 50 条
  • [21] Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation
    J. Prestel
    K. Gempel
    T. K. Hauser
    K. Schweitzer
    H. Prokisch
    U. Ahting
    D. Freudenstein
    E. Bueltmann
    T. Naegele
    D. Berg
    T. Klopstock
    T. Gasser
    Journal of Neurology, 2008, 255 : 643 - 648
  • [22] Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation
    Prestel, Juergen
    Gempel, Klaus
    Hauser, Till-Karsten
    Schweitzer, Katherine
    Prokisch, Holger
    Ahting, Uwe
    Freudenstein, Dirk
    Bueltmann, Eva
    Naegele, Thomas
    Berg, Daniela
    Klopstock, Thomas
    Gasser, Thomas
    JOURNAL OF NEUROLOGY, 2008, 255 (05) : 643 - 648
  • [23] Role of Pink1 in Parkinson's Disease and Mitochondrial Function: Pink1 Regulates Complex I Activity
    Morais, V. A.
    Craessaerts, K.
    Snellinx, A.
    Overbergh, L.
    Helbig, A. O.
    Heck, A. J. R.
    Mandemakers, W.
    Wurst, W.
    De Strooper, B.
    MOVEMENT DISORDERS, 2010, 25 : S625 - S625
  • [24] Analysis of PARKIN, PINK1 and DJ-1 mutation in an early-onset Parkinson's disease Korean cohort
    Kim, Y. J.
    Woo, M.
    Choi, J.
    Ma, H.
    Lee, P.
    Chung, S.
    Kim, J.
    Kang, S. Y.
    Shin, H.
    Lyoo, C.
    Sohn, Y.
    Kim, J.
    Kim, J.
    Lee, M.
    Lee, M.
    MOVEMENT DISORDERS, 2006, 21 : S406 - S407
  • [25] Pink1 heterozygous mutations in familial Parkinson's disease
    Hayashida, A.
    Li, Y.
    Yoshino, H.
    Nakahara, T.
    Yoritaka, A.
    Nagara, Y.
    Sakiyama, Y.
    Kusaka, H.
    Takiyama, Y.
    Morimoto, N.
    Uchino, A.
    Fujimoto, T.
    Sekijima, Y.
    Tomimoto, H.
    Tsuruta, K.
    Hattori, Y.
    Kashihara, K.
    Funayama, M.
    Nishioka, K.
    Hattori, N.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 161 - +
  • [26] Heterozygous PINK1 mutations:: A susceptibility factor for Parkinson disease?
    Djarmati, Ana
    Hedrich, Katja
    Svetel, Marina
    Lohnau, Thora
    Schwinger, Eberhard
    Romac, Stanka
    Pramstaller, Peter P.
    Kostic, Vladimir
    Klein, Christine
    MOVEMENT DISORDERS, 2006, 21 (09) : 1526 - 1530
  • [27] PARKINSON'S DISEASE Vivid views of the PINK1 protein
    Daou, Salima
    Sicheri, Frank
    NATURE, 2017, 552 (7683) : 38 - 39
  • [28] PINK1: a novel mitochondrial protein in Parkinson's disease
    Gandhi, S
    Muqit, MMK
    Abou-Sleiman, PM
    Stanyer, L
    Hargreaves, I
    Heales, S
    Ganguly, M
    Latchman, DS
    Holton, J
    Wood, NW
    Revesz, T
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2006, 32 (02) : 221 - 222
  • [29] A heterozygous effect for PINK1 mutations in Parkinson's disease?
    Abou-Sleiman, Patrick M.
    Muqit, Miratul M. K.
    McDonald, Neil Q.
    Yang, Yan Xiang
    Gandhi, Sonia
    Healy, Daniel G.
    Harvey, Kirsten
    Harvey, Robert J.
    Deas, Emma
    Hatia, Kailash
    Quinn, Niall
    Lees, Andrew
    Latchman, David S.
    Wood, Nicholas W.
    ANNALS OF NEUROLOGY, 2006, 60 (04) : 414 - 419
  • [30] Comprehensive assessment of PINK1 variants in Parkinson's disease
    Krohn, Lynne
    Grenn, Francis P.
    Makarious, Mary B.
    Kim, Jonggeol Jeffrey
    Bandres-Ciga, Sara
    Roosen, Dorien A.
    Gan-Or, Ziv
    Nalls, Mike A.
    Singleton, Andrew B.
    Blauwendraat, Cornelis
    NEUROBIOLOGY OF AGING, 2020, 91 : 168.e1 - 168.e5