# A novel truncating variant in PRDM16 causes severe familial cardiomyopathy with variable clinical presentations

**Authors:** Yuan Che, Lindsey Walker, Lillian Sau, Tingting Tang, Wei Li, Chao Shen, Nick Shillingford, Ramzi Bawab, Jianjun Chen, Miao Sun

PMC · DOI: 10.1016/j.gendis.2025.101879 · Genes & Diseases · 2025-10-13

## Full-text entities

- **Genes:** PRDM16 (PR/SET domain 16) [NCBI Gene 63976] {aka CMD1LL, KMT8F, LVNC8, MEL1, PFM13}
- **Diseases:** cardiomyopathy (MESH:D009202)

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