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Absence of p.R50X Pygm read-through in McArdle disease cellular models / Tarrasó, Guillermo (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Real-Martinez, Alberto (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Parés, Marta (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Romero-Cortadellas, Lídia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Puigros, Laura (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Moya Borrego, Laura (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; de Luna Salva, Noemí (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Brull, Astrid (Sorbonne Université, INSERM UMRS_974, Center of Research in Myology) ; Martín, Miguel Angel (Centro de Investigación Biomédica en Red de Enfermedades Raras) ; Arenas, Joaquín (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Lucia, Alejandro (European University) ; Andreu Périz, Antoni Lluís (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Barquinero, Jordi (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Vissing, John (Copenhagen University Hospital Rigshospitalet) ; Krag, Thomas (Copenhagen University Hospital Rigshospitalet) ; Pinós Figueras, Tomàs (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Universitat Autònoma de Barcelona
McArdle disease is an autosomal recessive disorder caused by the absence of muscle glycogen phosphorylase, which leads to blocked muscle glycogen breakdown. We used three different cellular models to evaluate the efficiency of different read-through agents (including amlexanox, Ataluren, RTC13 and G418) in McArdle disease. [...]
2020 - DOI (Digital Object Identifier)

10.1242/dmm.043281
Disease Models & Mechanisms, Vol. 13 (january 2020)

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