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Hereditary Frontotemporal Dementia Linked to the Pathogenic p.L266V Variant of the MAPT Gene in Korea

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참고문헌 (6)

  1. McKhann GM, "Clinical and pathological diagnosis of frontotemporal dementia : report of the Work Group on Frontotemporal Dementia and Pick’s Disease", Arch Neurol, 58, pp.1803~1809 (2001)
  2. Greaves CV, "An update on genetic frontotemporal dementia", J Neurol, 266, pp.2075~2086 (2019)
  3. Hutton M, "Association of missense and 5’-splice-site mutations in tau with the inherited dementia FTDP-17", Nature, 393, pp.702~705 (1998)
  4. Kobayashi T, "A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology", Ann Neurol, 53, pp.133~137 (2003)
  5. Kim EJ, "Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia", Neurobiol Aging, 35, pp.1213~ (2014)
  6. Kim EJ, "Analysis of frontotemporal dementia, amyotrophic lateral sclerosis, and other dementia-related genes in 107 Korean patients with frontotemporal dementia", Neurobiol Aging, 72, pp.186~ (2018)

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