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N D Pantzaris

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Kostopoulou E, Spilioti D, Pantzaris N, Spiliotis B
Eur Rev Med Pharmacol Sci . 2022 Apr; 26(7):2437-2442. PMID: 35442499
Objective: Prader-Willi syndrome (PWS) is a genomic imprinting disorder predominantly caused by the absence of paternally expressed imprinted genes at chromosome 15q11.2-q13. The PCSK1 gene is vital for the processing...