Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease

✍ Scribed by Synofzik, Matthis; Born, Christoph; Rominger, Axel; Lummel, Nina; Schöls, Ludger; Biskup, Saskia; Schüle, Cornelius; Grasshoff, Ute; Klopstock, Thomas; Adamczyk, Christopher

• Book ID: 122195458
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 651 KB
• Volume: 35
• Category: Article
• ISSN: 0197-4580
• DOI: 10.1016/j.neurobiolaging.2013.10.092