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...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:American journal of human genetics Ročník 111; číslo 7; s. 1352
Hlavní autori: 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
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 11.07.2024
Predmet:
ISSN:1537-6605, 1537-6605
On-line prístup:Zistit podrobnosti o prístupe
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Buďte prvý, kto okomentuje tento záznam!
Najprv sa musíte prihlásiť.