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Rare Diseases Volume 1, 2013 - Issue 1
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Addendum

Leptin signaling defects in a mouse model of Prader-Willi syndrome

An orphan genetic obesity syndrome no more?

William F. Colmers Department of Pharmacology; University of Alberta; Edmonton, AB Canada
&
Rachel Wevrick Department of Medical Genetics; University of Alberta; Edmonton, AB CanadaCorrespondence[email protected]
Article: e24421 | Received 27 Feb 2013, Accepted 22 Mar 2013, Published online: 27 Mar 2013

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