HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

Please use this identifier to cite or link to this item: http://ir.sinica.edu.tw/handle/201000000A/21526

Title:	HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
Authors:	Mukherjee, O. Pastor, P. Cairns, N. J. Chakraverty, S. Kauwe, J. S. Shears, S. Behrens, M. I. Budde, J. Hinrichs, A. L. Norton, J. Levitch, D. Taylor-Reinwald, L. Gitcho, M. Tu, P. H. Tenenholz Grinberg, L. Liscic, R. M. Armendariz, J. Morris, J. C. Goate, A. M.
Issue Date:	2006
Relation:	Ann Neurol 60(3), 314-322
URI:	http://ir.sinica.edu.tw/handle/201000000A/21526
ISSN:	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0364-5134&DestApp=JCR&RQ=IF_CAT_BOXPLOT
URL:	http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16983685
Appears in Collections:	生物醫學科學研究所

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