A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts-Reference-Cited by-同舟云学术

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A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts

Published:2013-06 Issue:6 Volume:34 Page:1708.e1-1708.e6
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Ingre Caroline,Landers John E.,Rizik Naji,Volk Alexander E.,Akimoto Chizuru,Birve Anna,Hübers Annemarie,Keagle Pamela J.,Piotrowska Katarzyna,Press Rayomand,Andersen Peter Munch,Ludolph Albert C.,Weishaupt Jochen H.

Funder

German Federal Ministry of Education and Research

Charcot Foundation for ALS Research

Swedish Brain Power Consortium

Swedish Brain Research Foundation

Bertil Hållsten Research Foundation

NIH/NINDS

Swabian ALS Registry

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference34 articles.

1. “True” sporadic ALS associated with a novel SOD-1 mutation;Alexander;Ann. Neurol.,2002

2. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?;Andersen;Nat. Rev. Neurol.,2011

3. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph. Lateral Scler. Other Motor Neuron Disord,2000

4. Proposed criteria for familial amyotrophic lateral sclerosis;Byrne;Amyotroph. Lateral Scler.,2011

5. Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene;Chio;Arch. Neurol.,2011

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