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Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

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Beckwith-Wiedemann syndrome (BWS) is a fetal overgrowth and human imprinting disorder resulting from the deregulation of a number of genes. including IGF2 and CDKN1C. in the imprinted gene cluster on chromosome 11p15. 5. https://www.mariameetsanna.com/product-category/liquid-body-makeup/
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