TRAPPC2
Abstract
Identification of a novel deletion variant in TRAPPC2 in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda
Fields of Study & Subjects
Connective tissue disorders research
Genomics and Rare Diseases
Osteoarthritis Treatment and Mechanisms
Publication details
- Journal / source
- Figshare
- Publication date
- 1 January 2026
- Document type
- Dataset