Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations-Reference-Cited by-同舟云学术

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

Published:2008-01-11 Issue:3 Volume:131 Page:721-731
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Pickering-Brown Stuart M.,Rollinson Sara,Du Plessis Daniel,Morrison Karen E.,Varma Anoop,Richardson Anna M. T.,Neary David,Snowden Julie S.,Mann David M. A.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/131/3/721/13735205/awm331.pdf

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5. A noveldeletion in progranulin gene is associated with FTDP-17 and CBS;Benussi;Neurobiol Aging,2006

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