E-mail a Wiley Online Library Link

Odity Mukherjee, Pau Pastor, Nigel J. Cairns, Sumi Chakraverty, John S. K. Kauwe, Shantia Shears, Maria I. Behrens, John Budde, Anthony L. Hinrichs, Joanne Norton, Denise Levitch, Lisa Taylor-Reinwald, Michael Gitcho, P.-H. Tu, Lea Tenenholz Grinberg, Rajka M. Liscic, Javier Armendariz, John C. Morris and Alison M. Goate HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin Annals of Neurology 60

Version of Record online: 18 SEP 2006 | DOI: 10.1002/ana.20963

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field