GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak-Reference-Cited by-同舟云学术

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak

Published:2008-05-01 Issue:6 Volume:118 Page:2157-2168
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Weber Yvonne G.,Storch Alexander,Wuttke Thomas V.,Brockmann Knut,Kempfle Judith,Maljevic Snezana,Margari Lucia,Kamm Christoph,Schneider Susanne A.,Huber Stephan M.,Pekrun Arnulf,Roebling Robert,Seebohm Guiscard,Koka Saisudha,Lang Camelia,Kraft Eduard,Blazevic Dragica,Salvo-Vargas Alberto,Fauler Michael,Mottaghy Felix M.,Münchau Alexander,Edwards Mark J.,Presicci Anna,Margari Francesco,Gasser Thomas,Lang Florian,Bhatia Kailash P.,Lehmann-Horn Frank,Lerche Holger

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference40 articles.

1. Familial (Idiopathic) Paroxysmal Dyskinesias: An Update

2. A Gene for Autosomal Dominant Paroxysmal Choreoathetosis/Spasticity (CSE) Maps to the Vicinity of a Potassium Channel Gene Cluster on Chromosome 1p, Probably within 2 cM between D1S443 and D1S197

3. Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16

4. Autosomal recessive Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12-11.2

5. Movement disorders following lesions of the thalamus or subthalamic region

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