# Correction: BAG3-related myofibrillar myopathy: focus on its cardiac involvement

**Authors:** Elise Daire, Elena Panaioli, Cyril Gitiaux, Catherine Gardin, Victor Waldmann, Damien Bonnet, Karim Wahbi, Diala Khraiche

PMC · DOI: 10.3389/fgene.2026.1786473 · Frontiers in Genetics · 2026-02-09

## Full-text entities

- **Genes:** BAG3 (BAG cochaperone 3) [NCBI Gene 9531] {aka BAG-3, BIS, CAIR-1, CMD1HH, CMT2JJ, HMND15}
- **Diseases:** heart failure (MESH:D006333), Hypertrophic cardiomyopathy (MESH:D002312), QT interval (OMIM:610141), Cardiac involvement (MESH:D006331), Restrictive cardiomyopathy (MESH:D002313), long or borderline QT interval (MESH:D008133), axonal neuropathy (MESH:D020269), ventricular hypertrophy (MESH:D024741), sudden death (MESH:D003645), hypertrophy (MESH:D006984), heart murmur (MESH:D006337), Gait disturbances (MESH:D020233), ventricular arrhythmias (MESH:D001145), chest pain (MESH:D002637), cardiomyopathy (MESH:D009202), HCM (MESH:D000092183), Neurological (MESH:D009461), myofibrillar myopathy (MESH:C580316), RCM (MESH:C566168), muscle weakness (MESH:D018908)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** p.Pro209Leu

## Full text

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Source: https://tomesphere.com/paper/PMC12926653