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

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

Published:2006-09 Issue:3 Volume:60 Page:314-322
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Mukherjee Odity,Pastor Pau,Cairns Nigel J.,Chakraverty Sumi,Kauwe John S. K.,Shears Shantia,Behrens Maria I.,Budde John,Hinrichs Anthony L.,Norton Joanne,Levitch Denise,Taylor-Reinwald Lisa,Gitcho Michael,Tu P.-H.,Tenenholz Grinberg Lea,Liscic Rajka M.,Armendariz Javier,Morris John C.,Goate Alison M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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