Impaired melanocortin pathway function in Prader–Willi syndrome gene-Magel2 deficient mice

Overview of attention for article published in Human Molecular Genetics, June 2018

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RT @zenbrainest: Impaired melanocortin pathway function in Prader-Willi Syndrome gene- Magel2 deficient mice | Human Molecular Genetics |…

Impaired melanocortin pathway function in Prader-Willi Syndrome gene- Magel2 deficient mice | Human Molecular Genetics | Oxford Academic https://t.co/jumpqR1FDy

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