Deml et al., 2015
- EFTUD2 deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish model.
Birth defects research. Part A, Clinical and molecular teratology
103(7):630-40
Full text @ Birth Defects Res. Part A Clin. Mol. Teratol.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | eef1a1l2 | eukaryotic translation elongation factor 1 alpha 1, like 2 |
| Gene | eftud2 | elongation factor Tu GTP binding domain containing 2 |