Novel LRRK2 mutation in the Roc domain in an Western Australian family with autosomal dominant late-onset Parkinson's disease (LOPD)

被引：0
|
作者：
Mastaglia, F. L.
Huang, Y.
Halliday, G. M.
Rowe, D. B.
Sue, C. M.
机构：
来源：
MOVEMENT DISORDERS | 2007年 / 22卷
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：
729
引用
收藏
页码：S224 / S224
页数：1
相关论文
共 50 条
  • [41] Is there an antagonistic pleiotropic effect of a LRRK2 mutation on leprosy and Parkinson's disease?
    Zhang, Deng-Feng
    Wang, Dong
    Li, Yu-Ye
    Yao, Yong-Gang
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (19) : 10122 - 10123
  • [42] Possible Link Between Crohn's Disease and LRRK2 Mutation Parkinson's Disease
    Ortega, Roberto A.
    Mirelman, Anat
    Pont-Sunyer, Claustre
    Vilas, Dolores
    Brockmann, Kathrin
    Waro, Bjorg
    Aasly, Jan
    Marder, Karen
    Berg, Daniela
    Foroud, Tatiana
    Tolosa, Eduardo
    Giladi, Nir
    Agalliu, Ilir
    Bressman, Susan B.
    Saunders-Pullman, Rachel
    ANNALS OF NEUROLOGY, 2017, 82 : S178 - S178
  • [43] Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact
    Sun, Yi-Min
    Gan, Lin-Hua
    Peng, Fang
    Zhou, Xin-Yue
    Chen, Qi-Si
    Liu, Feng-Tao
    Tang, Yi-Lin
    Wu, Ping
    Lu, Jia-Ying
    Ge, Jing-Jie
    Yen, Tzu-Chen
    Zuo, Chuan-Tao
    Song, Bin
    Wu, Jian-Jun
    Wang, Jian
    PARKINSONISM & RELATED DISORDERS, 2023, 111
  • [44] Dominant-negative effects of LRRK2 heterodimers: A possible mechanism of neurodegeneration in Parkinson's disease caused by LRRK2 I2020T mutation
    Ohta, Etsuro
    Kawakami, Fumitaka
    Kubo, Makoto
    Obata, Fumiya
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 430 (02) : 560 - 566
  • [45] A novel P755L mutation in LRRK2 gene associated with Parkinson's disease
    Wu, Ting
    Zeng, Yanying
    Ding, Xinsheng
    Li, Xiaobo
    Li, Wenlei
    Dong, Hairong
    Chen, Senqing
    Zhang, Xiaomei
    Ma, Guojian
    Yao, Juan
    Deng, Xiaoxuan
    NEUROREPORT, 2006, 17 (18) : 1859 - 1862
  • [46] Development of Novel Radioligands for Imaging LRRK2 in Parkinson's Disease
    Malik, Noeen
    Tuchman, Daniel
    Sandell, Johan
    Gifford, Andrew
    Ding, Yu-Shin
    JOURNAL OF NUCLEAR MEDICINE, 2018, 59
  • [47] GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment
    Ruiz-Martinez, Javier
    Krebs, Catharine E.
    Makarov, Vladimir
    Gorostidi, Ana
    Marti-Masso, Jose Felix
    Paisan-Ruiz, Coro
    JOURNAL OF HUMAN GENETICS, 2015, 60 (10) : 637 - 640
  • [48] GIGYF2 mutation in late-onset Parkinson’s disease with cognitive impairment
    Javier Ruiz-Martinez
    Catharine E Krebs
    Vladimir Makarov
    Ana Gorostidi
    Jose Félix Martí-Massó
    Coro Paisán-Ruiz
    Journal of Human Genetics, 2015, 60 : 637 - 640
  • [49] Missense mutations in the leucine-rich repeat kinase 2 (LRRK2) gene can cause late-onset Parkinson disease
    Daher, J. P. L.
    BRAIN PATHOLOGY, 2014, 24 : 71 - 72
  • [50] Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil
    Abreu, Gabriella de M.
    Valenca, Debora Cristina T.
    Campos Junior, Mario
    da Silva, Camilla P.
    Pereira, Joao S.
    Araujo Leite, Marco A.
    Rosso, Ana Lucia
    Nicaretta, Denise H.
    Vasconcellos, Luiz Felipe R.
    da Silva, Delson Jose
    Della Coletta, Marcus V.
    dos Santos, Jussara M.
    Goncalves, Andressa P.
    Santos-Reboucas, Cintia B.
    Pimentel, Marcia M. G.
    NEUROSCIENCE LETTERS, 2016, 635 : 67 - 70
12345