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Arrhythmias in patients with X-linked myotubular myopathy

INTRODUCTION. Myotubular myopathy is a congenital muscle disease caused by a mutation in the myotubularin (MTM1) gene. The X-linked myotubular myopathy (XLMTM) affects males with early-onset symptoms such as muscle weakness, hypotonia, and respiratory distress. To our knowledge, cardiac involvement...

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Detalles Bibliográficos
Autores principales:	Pons-Espinal, Marina, Clotet-Caba, Jordi, Cesar-Díaz, Sergi, Yubero-Siles, Delia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	EVIDENZE 2023
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662247/ https://www.ncbi.nlm.nih.gov/pubmed/37466134 http://dx.doi.org/10.33588/rn.7703.2022222

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