Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.
Bonnefond, Amélie; Raimondo, Anne; Stutzmann, Fanny; Ghoussaini, Maya; Ramachandrappa, Shwetha; Bersten, David C.; Durand, Emmanuelle; Vatin, Vincent; Balkau, Beverley; Lantieri, Olivier; Raverdy, Violeta; Pattou, François; Van Hul, Wim; Van Gaal, Luc; Peet, Daniel J.; Weill, Jacques; Miller, Jennifer L.; Horber, Fritz; Goldstone, Anthony P.; Driscoll, Daniel J.; Journal of Clinical Investigation, 2013, vol. 123, issue 7, p 3037, ISSN 00219738. ISBN 00219738.

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