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11 | Human immortalized myoblasts/induced pluripotent stem cell derived skeletal muscle model to investigate cystinosis myopathy

Cystinosis myopathy develops in cystinosis patients with CTNS mutations as the disease progresses despite cysteamine therapy or kidney transplantation. It presents as muscle weakness in distal, swallowing and respiratory muscles1. Muscle biopsy typically reveals autophagic vacuoles and cystine cryst...

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Autor principal: Interuniversity Institute of Myology
Format: Artigo
Idioma:Inglês
Publicat: PAGEPress Publications 2026-04-01
Col·lecció:European Journal of Translational Myology
Accés en línia:https://www.pagepressjournals.org/bam/article/view/15459
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