Snijders Blok et al., 2015
- Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
American journal of human genetics
97(2):343-52
Full text @ Am. J. Hum. Genet.
| Human Disease | Fish | Environment | Evidence Code |
|---|---|---|---|
| intellectual disability |