PDF) Hypothalamic loss of Snord116 recapitulates the hyperphagia
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Frontiers Epigenetics in Prader-Willi Syndrome
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Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome. - Abstract - Europe PMC
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction - The Lancet Diabetes & Endocrinology
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Murine neuronatin deficiency is associated with a hypervariable food intake and bimodal obesity
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SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome - Correa‐da‐Silva - 2021 - Journal of Neuroendocrinology - Wiley Online Library
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