Myofibrillar Myopathies: A Clinical and Myopathological Guide
Author:
Publisher
Wiley
Subject
Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience
Reference47 articles.
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3. Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation;Bär;Exp Cell Res,2006
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1. Desmin and its molecular chaperone, the αB-crystallin: How post-translational modifications modulate their functions in heart and skeletal muscles?;Biochimie;2024-01
2. Functional Characterization of a Novel Genetic Variant in Desmin (p.Glu353dup) Causing Myofibrillar Myopathy and Generation of Patient-Derived Induced Pluripotent Stem Cells for Disease Modeling;2023-12-28
3. Anaesthetic management of caesarean section in a patient with myofibrillar myopathy;BMJ Case Reports;2023-12
4. Human Mutated MYOT and CRYAB Genes Cause a Myopathic Phenotype in Zebrafish;International Journal of Molecular Sciences;2023-07-14
5. Myofibrillar myopathy hallmarks associated with ZAK deficiency;Human Molecular Genetics;2023-07-10
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