Closing the tau loop: the missing tau mutation-Reference-Cited by-同舟云学术

Closing the tau loop: the missing tau mutation

Published:2015-08-21 Issue:10 Volume:138 Page:3100-3109
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

McCarthy Allan,Lonergan Roisin,Olszewska Diana A.,O’Dowd Sean,Cummins Gemma,Magennis Brian,Fallon Emer M.,Pender Niall,Huey Edward D.,Cosentino Stephanie,O’Rourke Killian,Kelly Brendan D.,O’Connell Martin,Delon Isabelle,Farrell Michael,Spillantini Maria Grazia,Rowland Lewis P.,Fahn Stanley,Craig Peter,Hutton Michael,Lynch Tim

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/138/10/3100/13798831/awv234.pdf

Reference44 articles.

1. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

2. Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series

3. Comparison of 2 Diagnostic Criteria for the Behavioral Variant of Frontotemporal Dementia

4. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

5. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

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