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Deep Mutational Scanning and High-throughput Functional Testing to Resolve Variants of Unknown Significance in Sarcoglycanopathies

Author:Haller, Gabe   Li, Chengcheng   Weihl, Conrad   

Session Name:N4: Neuroscience in the Clinic: Bridging Genetics to the Clinic in Neuromuscular Disease  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:N4.001  

Author Institution:Washington University, St. Louis, MO  Washington University in St. Louis, St. Louis, MO