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

• Asıl Yazarlar: Catherine Takeda-Raguin (Yazar), Pierre Olivier Lang (Yazar), Jérémie Perisse (Yazar), Nathalie Philippi (Yazar), Patrick Karcher (Yazar), Thomas Vogel (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Archive of Gerontology and Geriatrics Research - Peertechz Publications, 2017-01-24.
• Konular: Case Report
• Online Erişim: Connect to this object online.

<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...