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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and familiesLan Xiong, Patrick Dion, Jacques Montplaisir, et al.The Journal of Biological Chemistry|June 2, 2011
Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosumAdèle Salin-Cantegrel, Jean-Baptiste Rivière, Masoud Shekarabi, et al.Human Molecular Genetics|February 17, 2012
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron modelsShawn J Stochmanski, Martine Therrien, Janet Laganière, et al.Neurobiology of Disease|March 10, 2005
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in micePatrick Dion, Vijayalakshmi Shanmugam, Claudia Gaspar, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2008
Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1Anastasia Levchenko, Jacques-Yves Montplaisir, Géraldine Asselin, et al.Human Molecular Genetics|January 8, 2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levelsLan Xiong, Hélène Catoire, Patrick Dion, et al.Archives of Neurology|October 10, 2007
Asian origin for the worldwide-spread mutational event in Machado-Joseph diseaseSandra Martins, Francesc Calafell, Claudia Gaspar, et al.Pageof 3