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Dokumenttyp:
journal article 
Autor(en):
Schumacher, A; Friedrich, P; Diehl, J; Ibach, B; Schoepfer-Wendels, A; Mueller, JC; Konta, L; Laws, SM; Kurz, A; Foerstl, H; Riemenschneider, M 
Titel:
No association of common VCP variants with sporadic frontotemporal dementia. 
Abstract:
Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD). To investigate the role of this novel gene in sporadic forms of frontotemporal dementia (FTD), we genotyped 27 single nucleotide polymorphisms covering the entire VCP genomic region in 198 patients with sporadic FTD and 184 matched controls from Germany. No significant association could be demonstrated. There is no evidenc...    »
 
Zeitschriftentitel:
Neurobiol Aging 
Jahr:
2009 
Band / Volume:
30 
Heft / Issue:
Seitenangaben Beitrag:
333-5 
Sprache:
eng 
Print-ISSN:
0197-4580 
TUM Einrichtung:
r Psychiatrie und Psychotherapie