Publication | Open Access
Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene
34
Citations
31
References
2013
Year
Clinical DisordersMendelian DisorderGenetic DisorderGeneticsPathologyGenetic FactorUpf3b GeneUnderlying Genetic InteractionMolecular MedicineDisease Gene IdentificationMedicineSatb2 ActsNeurogenetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1