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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Cruts, Marc; Gijselinck, Ilse; van der Zee, Julie; Engelborghs, Sebastiaan; Wils, Hans; Pirici, Daniel; Rademakers, Rosa; Vandenberghe, Rik; Dermaut, Bart; Martin, Jean-Jacques; van Duijn, Cornelia; Peeters, Karin; Sciot, Raf; Santens, Patrick; De Pooter, Tim; Mattheijssens, Maria; Van den Broeck, Marleen; Cuijt, Ivy; Vennekens, Krist'l; De Deyn, Peter P; Kumar-Singh, Samir; Van Broeckhoven, Christine.
Affiliation
  • Cruts M; Neurodegenerative Brain Diseases Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, Universiteitsplein 1, BE-2610 Antwerpen, Belgium.
Nature ; 442(7105): 920-4, 2006 Aug 24.
Article in En | MEDLINE | ID: mdl-16862115
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Collection: 01-internacional Database: MEDLINE Main subject: Temporal Lobe / Chromosomes, Human, Pair 17 / Ubiquitin / Dementia / Intercellular Signaling Peptides and Proteins / Frontal Lobe / Mutation Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Nature Year: 2006 Document type: Article Affiliation country:
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Temporal Lobe / Chromosomes, Human, Pair 17 / Ubiquitin / Dementia / Intercellular Signaling Peptides and Proteins / Frontal Lobe / Mutation Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Nature Year: 2006 Document type: Article Affiliation country: