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Skeletal muscle delimited myopathy and verapamil toxicity in SUR2 mutant mouse models of AIMS
ABCC9‐related intellectual disability and myopathy syndrome (AIMS) arises from loss‐of‐function (LoF) mutations in the ABCC9 gene, which encodes the SUR2 subunit of ATP‐sensitive potassium (K(ATP)) channels. K(ATP) channels are found throughout the cardiovascular system and skeletal muscle and coupl...
Autores principales: | McClenaghan, Conor, Mukadam, Maya A, Roeglin, Jacob, Tryon, Robert C, Grabner, Manfred, Dayal, Anamika, Meyer, Gretchen A, Nichols, Colin G |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245035/ https://www.ncbi.nlm.nih.gov/pubmed/37154692 http://dx.doi.org/10.15252/emmm.202216883 |
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