Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation

Saved in:

Bibliographic Details
Published in:	Parkinsonism & related disorders Vol. 16; no. 7; pp. 484 - 485
Main Authors:	Di Fabio, Roberto, Tessa, Alessandra, Simons, Erik J, Santorelli, Filippo M, Casali, Carlo, Serrao, Mariano, Pierelli, Francesco, Bonifati, Vincenzo
Format:	Journal Article
Language:	English
Published:	England Elsevier Ltd 01-08-2010
Subjects:	Aged DNA Mutational Analysis - methods Family Health Female Frontotemporal dementia Frontotemporal Dementia - genetics GRN Humans Intercellular Signaling Peptides and Proteins - genetics Italy Male Middle Aged Mutation Mutation - genetics Neurology Parkinsonism Progranulin Italy Parkinsonism GRN Progranulin Mutation Frontotemporal dementia
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Bibliography:	SourceType-Other Sources-1 content type line 63 ObjectType-Correspondence-1 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23
ISSN:	1353-8020 1873-5126
DOI:	10.1016/j.parkreldis.2010.05.001