Title: | Mutant valosin-containing protein causes a novel type of frontotemporal dementia |
Journal : | Annals of neurology, 57, 3 |
Authors: | Schröder R ; Watts GDJ ; Mehta SG ; Evert BO ; Broich P ; Fliessbach K ; Pauls K ; Hans VH ; Kimonis V ; Thal DR |
Material Type: | Article |
Publication Date: | 2005 |
Size: | p. 457-461 |
Languages: | English |
Keywords : | autopsy ; autosomal dominant inheritance ; central nervous system ; chromosome 9 ; genetic mutations ; Germany ; histochemistry ; inclusion body myopathy with Paget disease and frontotemporal dementia ; molecular genetics ; VCP gene |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15732117&query_hl=19&itool=pubmed_docsum |