TARDBP p.I383V, a recurrent alteration in Greek FTD patients

Charoniti, E; Papastefanopoulou, V; Florou-Hatziyiannidou, C; Koros, C; Stanitsa, E; Papatriantafyllou, JD; Papageorgiou, SG; Kroupis, C

Papageorgiou, SG (corresponding author), Natl & Kapodistrian Univ Athens, Eginite Univ Hosp, Med Sch, Dept Neurol 1, Athens, Greece.

JOURNAL OF THE NEUROLOGICAL SCIENCES, 2021; 428 ():

Abstract

Background: A significant proportion of FTD (Frontotemporal Degeneration) cases can be attributed to mutations in major genes such as GRN, MAPT and C9......

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