Associated Papers
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
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure.
Weihl CC et al.
Acta Neuropathologica, 2023
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