Associated Papers
Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathy.
Inoue M et al.
Current Opinion in Neurology, 2025
Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure.
Chitimus DM et al.
Revue Neurologique, 2025
Molecular genetics of J-domain protein-related chaperonopathies in skeletal muscle.
Inoue M
Journal of Human Genetics, 2025
Structural-functional relevance of DNAJBs in protein aggregation and associated neurodegenerative diseases.
Fatima S et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics, 2025
Genotype‒phenotype correlation in recessive DNAJB4 myopathy.
Inoue M et al.
Acta Neuropathologica Communications, 2024
Genotype-phenotype correlation in recessive DNAJB4 myopathy.
Inoue M et al.
Research Square, 2024
Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches.
Findlay AR
Disease Models & Mechanisms, 2024
Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4.
Inoue M et al.
Acta Neuropathologica, 2023
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