Browse All

Current Filters

CLEAR FILTER x

TITLE

Brody myopathy associated with novel compound heterozygous ATP2A1 mutations

Author:Walia, Sargun   Su, Xiaowei   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P6.015  

Author Institution:Penn State Hershey Department of Neurology, Hershey , PA  Penn State Hershey Department of Neurology, Hershey, PA