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Case Report: Extent of the Clinical Spectrum for C9orf72 Mutation - From Frontotemporal Dementia to Autonomic Dysfunction

<p>C9ORF72 gene mutation on chromosome 9 corresponding to a repetition of hexanucleotides (GGGGCC) xn is the most common mutation found in frontotemporal lobar dementia (FTLD) and amyotrophic lateral sclerosis (SLA) [1]. FTLD is characterized by an insidious onset with gradual evolution, a dec...

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書誌詳細
主要な著者:	Catherine Takeda-Raguin (著者), Pierre Olivier Lang (著者), Jérémie Perisse (著者), Nathalie Philippi (著者), Patrick Karcher (著者), Thomas Vogel (著者)
フォーマット:	図書
出版事項:	Archive of Gerontology and Geriatrics Research - Peertechz Publications, 2017-01-24.
主題:	Case Report
オンライン･アクセス:	Connect to this object online.
タグ:	タグ追加タグなし, このレコードへの初めてのタグを付けませんか!

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