# Novel compound heterozygous TTN gene variants with additional potential contributory mutations in two sisters with severe scoliosis: A case report

**Authors:** Huaiyuan Wang, Shengjie Li, Weiyun Chen, Jianxiong Shen

PMC · DOI: 10.1016/j.gendis.2024.101477 · Genes & Diseases · 2024-12-03

## Full-text entities

- **Genes:** TTN (titin) [NCBI Gene 7273] {aka CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC}
- **Diseases:** scoliosis (MESH:D012600)

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