PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response

Primary proteasomopathies have recently emerged as a new class of rare early-onset neurodevelopmental disorders (NDDs) caused by pathogenic variants in the PSMB1, PSMC1, PSMC3, or PSMD12 proteasome genes. Proteasomes are large multi-subunit protein complexes that maintain cellular protein homeostasi...

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Veröffentlicht in:American journal of human genetics Jg. 111; H. 7; S. 1352
Hauptverfasser: Deb, Wallid, Rosenfelt, Cory, Vignard, Virginie, Papendorf, Jonas Johannes, Möller, Sophie, Wendlandt, Martin, Studencka-Turski, Maja, Cogné, Benjamin, Besnard, Thomas, Ruffier, Léa, Toutain, Bérénice, Poirier, Léa, Cuinat, Silvestre, Kritzer, Amy, Crunk, Amy, diMonda, Janette, Vengoechea, Jaime, Mercier, Sandra, Kleinendorst, Lotte, van Haelst, Mieke M, Zuurbier, Linda, Sulem, Telma, Katrínardóttir, Hildigunnur, Friðriksdóttir, Rún, Sulem, Patrick, Stefansson, Kari, Jonsdottir, Berglind, Zeidler, Shimriet, Sinnema, Margje, Stegmann, Alexander P A, Naveh, Natali, Skraban, Cara M, Gray, Christopher, Murrell, Jill R, Isikay, Sedat, Pehlivan, Davut, Calame, Daniel G, Posey, Jennifer E, Nizon, Mathilde, McWalter, Kirsty, Lupski, James R, Isidor, Bertrand, Bolduc, François V, Bézieau, Stéphane, Krüger, Elke, Küry, Sébastien, Ebstein, Frédéric
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 11.07.2024
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ISSN:1537-6605, 1537-6605
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