Associated Papers
Molecular genetics of J-domain protein-related chaperonopathies in skeletal muscle.
Inoue M
Journal of Human Genetics, 2025
A female carrier of spinal and bulbar muscular atrophy diagnosed with DNAJB6-related distal myopathy.
Xu L et al.
Journal of Human Genetics, 2022
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.
Sarparanta J et al.
International Journal of Molecular Sciences, 2020
Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations.
Finsterer J
Yonsei Medical Journal, 2018
The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations.
Kim K et al.
Yonsei Medical Journal, 2018
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation.
Bohlega SA et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families.
Jonson PH et al.
European Journal of Neurology, 2018
Select a paper to view details