ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disorders

Abstract Introduction Imprinting disorders (IDs) are a rare class of diseases caused by the disruption of imprinted genes, i.e., genes with a specific pattern of expression from only one allele. Currently, 48 loci are known to show parent-of-origin dependent, imprinted, expression in humans, some of...

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Bibliographic Details
Main Authors: Frédéric Brioude, Martin A. Haagmans, Marcel Mannens, Irene Netchine, Marielle Alders, Peter Henneman, Jet Bliek
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Clinical Epigenetics
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Online Access:https://doi.org/10.1186/s13148-025-01916-x
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