The de novo CACNA1A pathogenic variant Y1384C associated with hemiplegic migraine, early onset cerebellar atrophy and developmental delay leads to a loss of Cav2.1 channel function

RT @TheWeissLab: The de novo #CACNA1A pathogenic variant Y1384C associated with hemiplegic #migraine, cerebellar atrophy and developmental…

RT @TheWeissLab: The de novo #CACNA1A pathogenic variant Y1384C associated with hemiplegic #migraine, cerebellar atrophy and developmental…

The de novo #CACNA1A pathogenic variant Y1384C associated with hemiplegic #migraine, cerebellar atrophy and developmental delay leads to a loss of Cav2.1 #calcium #ionchannels function ➡️ https://t.co/ZVPWqVfNT0 https://t.co/oz6fc8XssE

New Article: The de novo CACNA1A pathogenic variant Y1384C associated with hemiplegic migraine, early onset cerebellar atrophy and developmental delay leads to a loss of Cav2.1 channel function https://t.co/qPonGfRCSK