Work

Investigation of a Novel Mouse Model of Prader-Willi Syndrome with Invalidation of Necdin and Magel2

Year: 2024

Type: preprint

Source: bioRxiv (Cold Spring Harbor Laboratory)

DOI: 10.1101/2024.07.24.604909

Authors: Pierre-Yves Barelle, Alicia Sicardi, Fabienne Schaller, Julie Buron, Denis Becquet, Felix Omnes, Françoise Watrin, Catarina Santos, Clément Menuet, Anne-Marie François-Bellan, Emilie Caron, Jessica Klucznik, Vincent Prevot, Sebastien G Bouret, Françoise Muscatelli

Institutions: Inserm, Université de Lille, Centre Hospitalier Universitaire de Lille, Lille Neurosciences & Cognition, Aix-Marseille Université, Institut de Neurobiologie de la Méditerranée, Institut de Neurophysiopathologie

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4400933479

Cites: 81

Cited by: 2

Related to: 10