COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum.
Omid HesamiMahtab RamezaniAida GhasemiFarzad FatehiAli Asghar OkhovatBentolhoda ZiaadiniAriana KariminejadShahriar NafissiPublished in: Orphanet journal of rare diseases (2024)
Despite the rarity of the disease, our findings provide valuable information for understanding the clinical and electrophysiological features as well as the genetic characterization and response to the treatment of COLQ-CMS.
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