Dysarthria leads diagnosis in teen with Becker myotonia and CLCN1 variant
A case report describes a 13-year-old Persian boy whose genetically confirmed Becker-type myotonia congenita presented primarily as dysarthria.
A case report describes a 13-year-old Persian boy whose genetically confirmed Becker-type myotonia congenita presented primarily as dysarthria.
A case report describes a 64-year-old woman with multiple myeloma and an SCN5A overlap channelopathy who underwent autologous stem cell ...
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