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Clinical Heterogeneity in a Family With Rare F33L Hereditary Transthyretin Amyloidosis: A Case Series of Three Siblings

Author:Alhallaq, Lamees   Avila, J. David   

Session Name:P6: Neuromuscular and Clinical Neurophysiology (EMG): Peripheral Nerve and Other Neuromuscular Disorders  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P6.009  

Author Institution:Geisinger Medical Center, Bloomsburg, PA  Geisinger Medical Center, Danville, PA