TorsinA dysfunction causes persistent neuronal nuclear pore defects
Author:
Affiliation:
1. Department of Neurology
2. Cellular and Molecular Biology Program
3. Department of Cell and Developmental Biology
4. VA Ann Arbor Health System, University of Michigan Medical School, Ann Arbor, MI 48109, USA
Funder
National Institute of Neurological Disorders and Stroke
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/27/3/407/24325698/ddx405.pdf
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3. Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope;Goodchild;Neuron,2005
4. The DYT1 phenotype and guidelines for diagnostic testing;Bressman;Neurology,2000
5. Cerebellothalamocortical connectivity regulates penetrance in dystonia;Argyelan;J. Neurosci,2009
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