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Novel ACTA1 Mutation in a Family with Congenital Myopathy and Variably-penetrant Cardiomyopathy

Author:Putko, Brendan   Schmitt, Laura   Oudit, Gavin   Phan, Cecile   Beecher, Grayson   

Session Name:P6: Neuromuscular Disease: Inherited Muscle Disorders 3  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P6.008  

Author Institution:University of Alberta, Edmonton, AB, Canada