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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| Vydané v: | American journal of human genetics Ročník 111; číslo 7; s. 1352 |
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| Hlavní autori: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
United States
11.07.2024
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| Predmet: | |
| ISSN: | 1537-6605, 1537-6605 |
| On-line prístup: | Zistit podrobnosti o prístupe |
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