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Genes for Movement

Genes for Movement EDITORIAL The authors propose that the MR-1 gene plays a role Publisher’s Note: Because of a technical error in file in myofibril development through the regulation of cal- conversion, this editorial, originally published in the July cium or possibly other ion sequestration. Thus, they view issue of the ARCHIVES (2004;61:1006), was missing fi- PDC as resulting from abnormal ion localization, simi- nal sentences. The complete editorial is republished here lar to other episodic neurologic disorders. The finding and is also available free at the journal’s Web site: http:// of MR-1 as the gene that causes PDC is an important neu- archneur.ama-assn.org/cgi/content/full/61/7/1006. The rogenetic event. This finding will be an impetus for stud- journal regrets the error. ies to explain the effect of alcohol and caffeine on trig- gering paroxysmal movement attacks and, more centrally and specifically, why MR-1 mutations cause episodic ex- N 1940, MOUNT AND REBACK DESCRIBED FAMIL- trapyramidal involuntary movements. ial paroxysmal choreoathetosis in a report in the The question is often asked regarding whether or not ARCHIVES, more than 60 years ago. Known also the Human Genome Project (http://www.ornl.gov/sci as paroxysmal dystonic choreoathetosis (PDC) /techresources/Human_Genome/home.shtml; http:// I (Mendelian Inheritance in Man No. 11880) and www.ncbi.nlm.nih.gov/genome/guide/human/) has http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png JAMA Neurology American Medical Association

Genes for Movement

JAMA Neurology , Volume 61 (8) – Aug 1, 2004

Genes for Movement

Abstract

EDITORIAL The authors propose that the MR-1 gene plays a role Publisher’s Note: Because of a technical error in file in myofibril development through the regulation of cal- conversion, this editorial, originally published in the July cium or possibly other ion sequestration. Thus, they view issue of the ARCHIVES (2004;61:1006), was missing fi- PDC as resulting from abnormal ion localization, simi- nal sentences. The complete editorial is republished here lar to other episodic neurologic...
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Publisher
American Medical Association
Copyright
Copyright 2004 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.
ISSN
2168-6149
eISSN
2168-6157
DOI
10.1001/archneur.61.8.1182
pmid
15313833
Publisher site
See Article on Publisher Site

Abstract

EDITORIAL The authors propose that the MR-1 gene plays a role Publisher’s Note: Because of a technical error in file in myofibril development through the regulation of cal- conversion, this editorial, originally published in the July cium or possibly other ion sequestration. Thus, they view issue of the ARCHIVES (2004;61:1006), was missing fi- PDC as resulting from abnormal ion localization, simi- nal sentences. The complete editorial is republished here lar to other episodic neurologic disorders. The finding and is also available free at the journal’s Web site: http:// of MR-1 as the gene that causes PDC is an important neu- archneur.ama-assn.org/cgi/content/full/61/7/1006. The rogenetic event. This finding will be an impetus for stud- journal regrets the error. ies to explain the effect of alcohol and caffeine on trig- gering paroxysmal movement attacks and, more centrally and specifically, why MR-1 mutations cause episodic ex- N 1940, MOUNT AND REBACK DESCRIBED FAMIL- trapyramidal involuntary movements. ial paroxysmal choreoathetosis in a report in the The question is often asked regarding whether or not ARCHIVES, more than 60 years ago. Known also the Human Genome Project (http://www.ornl.gov/sci as paroxysmal dystonic choreoathetosis (PDC) /techresources/Human_Genome/home.shtml; http:// I (Mendelian Inheritance in Man No. 11880) and www.ncbi.nlm.nih.gov/genome/guide/human/) has

Journal

JAMA NeurologyAmerican Medical Association

Published: Aug 1, 2004

References