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UnknownBi-allelic variants in INTS11 are associated with a complex neurological disorder.
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S-EPMC10183469 | biostudies-literature
UnknownGain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
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S-EPMC9484401 | biostudies-literature
UnknownCardiovascular effects of intensive lifestyle intervention in type 2 diabetes.
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S-EPMC3791615 | biostudies-literature
UnknownA second update on mapping the human genetic architecture of COVID-19.
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S-EPMC10482689 | biostudies-literature
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