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Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis by Samah K. Aburahma, Liqa A. Rousan, Mohammad Shboul, Fabio Biella, Sabrina Lucchiari, Giacomo Pietro Comi, Giacomo Pietro Comi, Giovanni Meola, Giovanni Meola, Serena Pagliarani
Published 2024-02-01
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