Investigation of a mouse model of Prader-Willi syndrome with combined disruption of Necdin and Magel2.
Barelle PY, Sicardi A, Schaller F, Buron J, Becquet D, Omnes F, Watrin F, Alifrangis MS, Santos C, Menuet C, François-Bellan AM, Caron E, Klucznik J, Prevot V, Bouret SG, Muscatelli F
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