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Homozygous and Compound Heterozygous Mutations in the CLCN1 Gene Causes Myotonia in Two Related Saudi Families

Author:Pagliarani, Serena Alabdulwahed, Alwaleed Monfrini, Edoardo Lucchiari, Sabrina Comi, Giacomo Di Fonzo, Alessio AlAhmari, Aawadh Abulaban, Ahmed AlEyaid, Wafaa

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Myopathies

Topic:Neuromuscular and Clinical Neurophysiology (EMG)

Program Number:P2.032

Author Institution:Department of Neurology, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia, Riyadh, Saudi Arabia

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