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Volumn 44, Issue 1, 2015, Pages 277-282

The novel GRN g.1159-1160delTG mutation is associated with behavioral variant frontotemporal dementia

Author keywords

Deletion; Frontotemporal dementia; Haploinsufficiency; Mutation; Progranulin (GRN)

Indexed keywords

FLUORODEOXYGLUCOSE F 18; PROGRANULIN; GRN PROTEIN, HUMAN; SIGNAL PEPTIDE;

EID: 84920759172     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-141380     Document Type: Article
Times cited : (7)

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    • Evidence of presynaptic dopaminergic deficit in a patient with a novel progranulin mutation presenting with atypical parkinsonism
    • Carecchio M, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Comi C, Terazzi E, Cantello R (2012) Evidence of presynaptic dopaminergic deficit in a patient with a novel progranulin mutation presenting with atypical parkinsonism. J Alzheimers Dis 38, 747-752.
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    • Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.