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MAGEL2 protein
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Clinical characteristics and genetic analysis of a case of infantile Schaaf-Yang syndrome due to a h…
Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.
Dopamine pathway imbalance in mice lacking Magel2, a Prader-Willi syndrome candidate gene.
Subcellular localisation of truncated MAGEL2 proteins: insight into the molecular pathology of Schaa…
Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-nu…
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