Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders.
Saved in:
| Title: | Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders. |
|---|---|
| Authors: | Gimelli, Stefania1 stefania.gimelli@gmail.com, Capra, Valeria2 valeriacapra@ospedale-gaslini.ge.it, Rocco, Maja Di3 majadirocco@ospedale-gaslini.ge.it, Leoni, Massimiliano4 leonimassi@hotmail.com, Mirabelli-Badenier, Marisol5 marisol.mirabelli@gmail.com, Schiaffino, Maria6 mariacristinaschiaffino@ospedale-gaslini.ge.it, Fiorio, Patrizia7 patriziafiorio@ospedale-gaslini.ge.it, Cuoco, Cristina7 cristinacuoco@ospedale-gaslini.ge.it, Gimelli, Giorgio7 giorgio.gimelli@gmail.com, Tassano, Elisa7 eli.tassano@gmail.com |
| Source: | Molecular Cytogenetics (17558166). 2014, Vol. 7 Issue 1, p1-13. 13p. |
| Database: | Academic Search Ultimate |
Be the first to leave a comment!