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Loss of Magel2, a Candidate Gene for Features of Prader-Willi Syndrome, Impairs Reproductive Function in Mice

BACKGROUND: MAGEL2 is one of several genes typically inactivated in the developmental obesity disorder Prader-Willi syndrome (PWS). The physiological consequences of loss of MAGEL2, but without the concurrent loss of other PWS genes, are not well understood. Gene-targeted mutation of Magel2 in mice...

詳細記述

保存先:
書誌詳細
主要な著者: Mercer, Rebecca E., Wevrick, Rachel
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2627930/
https://ncbi.nlm.nih.gov/pubmed/19172181
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0004291
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