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Hyperphagia in Prader–Willi syndrome: linking hypothalamic dysfunction to clinical assessment and management across the lifespan2026 Orphanet Journal of Rare Diseases review Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
M. Tauber, Gwénaëlle Diene, Christine Poitou, Charlotte Höybye, Evelien F. Gevers, Anthony Peter Goldstone, +13 more
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