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Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders.

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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
Description
ISSN:17558166
DOI:10.1186/s13039-014-0054-y