PDF) Hypothalamic loss of Snord116 recapitulates the hyperphagia
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SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome - ScienceDirect
Frontiers Food socialization of children with Prader-Willi syndrome: an interdisciplinary problematization
Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes - Iiro Ilmari Salminen, Bernard J Crespi, Mikael Mokkonen, 2019
Frontiers Epigenetics in Prader-Willi Syndrome
Dysregulated adipose tissue expansion and impaired adipogenesis in Prader-Willi syndrome children before obesity-onset - ScienceDirect
SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
Frontiers Epigenetics in Prader-Willi Syndrome
Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome - Correa‐da‐Silva - 2021 - Journal of Neuroendocrinology - Wiley Online Library
Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction - The Lancet Diabetes & Endocrinology
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