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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 17, 2016 - Issue 3-4
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A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demon

Yu-Wen ChengDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan
,
Ming-Jen LeeDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan
,
Ta-Fu ChenDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan
,
Ting-Wen ChengDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan
,
Ya-Mei LaiDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan
,
Mau-Sun HuaDepartment of Psychology, College of Science, National Taiwan University, Taipei
&
Ming-Jang ChiuDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan;Department of Psychology, College of Science, National Taiwan University, Taipei;Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, TaiwanCorrespondence[email protected]
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Pages 292-294 | Received 20 May 2015, Accepted 13 Sep 2015, Published online: 19 Nov 2015

References

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  • Mosca L, Lunetta C, Tarlarini C, Avemaria F, Maestri E, Melazzini M, et al. Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject. Neurobiol Aging. 2012;33: 1846.e1–4.
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