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UnknownGWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.
Not available
S-EPMC10484785 | biostudies-literature
UnknownAMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Not available
S-EPMC6626132 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC11646479 | biostudies-literature
UnknownLapses in Care Among Patients Assigned to Ranibizumab for Proliferative Diabetic Retinopathy: A Post Hoc Analysis of a Randomized Clinical Trial.
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S-EPMC8532036 | biostudies-literature
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