Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis
病例报告:二氢吡啶受体(CACNA1S)先天性肌病,一种伴有早期发作周期性麻痹的新型表型
期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2024.1359479
Aburahma, Samah K; Rousan, Liqa A; Shboul, Mohammad; Biella, Fabio; Lucchiari, Sabrina; Comi, Giacomo Pietro; Meola, Giovanni; Pagliarani, Serena