Genetics of Parkinson's disease: alpha-synuclein and other insights from Greece

被引:3
作者
Proukakis, C. [1 ]
机构
[1] UCL Inst Neurol, Clin Neurosci Dept, London, England
关键词
MUTATION; PARK2;
D O I
10.1111/ene.12357
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:946 / 947
页数:2
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  • [1] Genetic assessment of familial and early-onset Parkinson's disease in a Greek population
    Bozi, M.
    Papadimitriou, D.
    Antonellou, R.
    Moraitou, M.
    Maniati, M.
    Vassilatis, D. K.
    Papageorgiou, S. G.
    Leonardos, A.
    Tagaris, G.
    Malamis, G.
    Theofilopoulos, D.
    Kamakari, S.
    Stamboulis, E.
    Hadjigeorgiou, G. M.
    Athanassiadou, A.
    Michelakakis, H.
    Papadimitriou, A.
    Gasser, T.
    Stefanis, L.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2014, 21 (07) : 963 - 968
  • [2] Pseudo-heterozygous rearrangement mutation of parkin
    Funayama, Manabu
    Yoshino, Hiroyo
    Li, Yuanzhe
    Kusaka, Hiromichi
    Tomiyama, Hiroyuki
    Hattori, Nobutaka
    [J]. MOVEMENT DISORDERS, 2012, 27 (04) : 552 - 555
  • [3] The many faces of alpha-synuclein mutations
    Kasten, Meike
    Klein, Christine
    [J]. MOVEMENT DISORDERS, 2013, 28 (06) : 697 - 701
  • [4] Copy Number Variation in Familial Parkinson Disease
    Pankratz, Nathan
    Dumitriu, Alexandra
    Hetrick, Kurt N.
    Sun, Mei
    Latourelle, Jeanne C.
    Wilk, Jemma B.
    Halter, Cheryl
    Doheny, Kimberly F.
    Gusella, James F.
    Nichols, William C.
    Myers, Richard H.
    Foroud, Tatiana
    DeStefano, Anita L.
    [J]. PLOS ONE, 2011, 6 (08):
  • [5] Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
    Polymeropoulos, MH
    Lavedan, C
    Leroy, E
    Ide, SE
    Dehejia, A
    Dutra, A
    Pike, B
    Root, H
    Rubenstein, J
    Boyer, R
    Stenroos, ES
    Chandrasekharappa, S
    Athanassiadou, A
    Papapetropoulos, T
    Johnson, WG
    Lazzarini, AM
    Duvoisin, RC
    DiIorio, G
    Golbe, LI
    Nussbaum, RL
    [J]. SCIENCE, 1997, 276 (5321) : 2045 - 2047
  • [6] Analysis of PARK2 Gene Exon Rearrangements in Russian Patients with Sporadic Parkinson's Disease
    Semenova, Elena V.
    Shadrina, Maria I.
    Slominsky, Pyotr A.
    Ivanova-Smolenskaya, Irina A.
    Bagyeva, Gulbakhar
    Illarioshkin, Sergei N.
    Limborska, Svetlana A.
    [J]. MOVEMENT DISORDERS, 2012, 27 (01) : 139 - 142
  • [7] Allelic Imbalance of Expression and Epigenetic Regulation within the Alpha-Synuclein Wild-Type and p.Ala53Thr Alleles in Parkinson Disease
    Voutsinas, Gerassimos E.
    Stavrou, Eleana F.
    Karousos, Gerassimos
    Dasoula, Aggeliki
    Papachatzopoulou, Adamantia
    Syrrou, Maria
    Verkerk, Annemieke J. M. H.
    van der Spek, Peter
    Patrinos, George P.
    Stoger, Reinhard
    Athanassiadou, Aglaia
    [J]. HUMAN MUTATION, 2010, 31 (06) : 685 - 691
  • [8] High-Resolution Survey in Familial Parkinson Disease Genes Reveals Multiple Independent Copy Number Variation Events in PARK2
    Wang, Liyong
    Nuytemans, Karen
    Bademci, Guney
    Jauregui, Cherylyn
    Martin, Eden R.
    Scott, William K.
    Vance, Jeffery M.
    Zuchner, Stephan
    [J]. HUMAN MUTATION, 2013, 34 (08) : 1071 - 1074