Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia

Author:

Mignarri Andrea,Battistini Stefania,Tomai Pitinca Maria Luigia,Monti Lucia,Burroni Luca,Ginanneschi Federica,Ricci Claudia,Bavazzano Antonio,Federico Antonio,Restagno Gabriella,Dotti Maria Teresa

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference10 articles.

1. The genetics and neuropathology of frontotemporal lobar degeneration;Sieben;Acta Neuropathol,2012

2. Screening for C9ORF72 repeat expansion in FTLD;Ferrari;Neurobiol Aging,1850

3. Mixed tau, TDP-43 and p62 pathology in FTLD associated with a C9ORF72 repeat expansion and p.Ala239Thr MAPT (tau) variant;King;Acta Neuropathol,2013

4. C9ORF72 repeat expansions in cases with previously identified pathogenic mutations;Van Blitterswijk;Neurology,2013

5. A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia;Lashley;Neuropathol Appl Neurobiol,2013

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