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J-GLOBAL ID：202002274442187280   Reference number：20A0052442

認知症の遺伝子研究のこれまでとこれから その他の認知症に関する遺伝子-DLB/PDD,紀伊ALS/PDCおよびHD-

Author (1)： KOKUBO YASUMASA (三重大 大学院地域イノベーション学研究科 紀伊神経難病研究セ)
Material： 老年精神医学雑誌  (Japanese Journal of Geriatric Psychiatry)
Volume： 30  Issue： 11  Page： 1253-1260  Publication year： Nov. 20, 2019 
JST Material Number： L1147A  ISSN： 0915-6305  Document type： Article
Article type： 解説  Country of issue： Japan (JPN)  Language： JAPANESE (JA)

Thesaurus term： Parkinson's disease ,...
Semi thesaurus term： *genetic variation ,...

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JST classification (2)： Basic neurology  (GN01020W) ,  Genetic variation  (EC01030Y)

Reference (52)：

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• Anheim M, Lagier-Tourenne C, Stevanin G, Fleury M, et al.: SPG11 spastic paraplegia ; A new cause of juvenile parkinsonism. J Neurol, 256 (1) : 104-108 (2009).
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• Behrens MI, Brüggemann N, Chana P, Venegas P, et al.: Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations. Mov Disord, 25 (12) : 1929-1937 (2010).
• Bras J, Verloes A, Schneider SA, Mole SE, et al.: Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Hum Mol Genet, 21 (12) : 2646-2650 (2012).

Terms in the title (7)： 認知症 ,  遺伝子 ,  研究 ,  PDD ,  ALS ,  PDC ,  HD