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UnknownDe novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities.
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S-EPMC11221546 | biostudies-literature
UnknownHeterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.
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S-EPMC8487929 | biostudies-literature
UnknownSocializing One Health: an innovative strategy to investigate social and behavioral risks of emerging viral threats.
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S-EPMC8122533 | biostudies-literature
UnknownCardiac manifestations and outcomes of COVID-19 vaccine-associated myocarditis in the young in the USA: longitudinal results from the Myocarditis After COVID Vaccination (MACiV) multicenter study.
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S-EPMC11406334 | biostudies-literature
UnknownGATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder.
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S-EPMC7920571 | biostudies-literature
UnknownHNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.
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S-EPMC10432175 | biostudies-literature
UnknownSafety of the PCSK9 inhibitor alirocumab: insights from 47 296 patient-years of observation.
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S-EPMC11249957 | biostudies-literature
UnknownThe clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
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S-EPMC10257005 | biostudies-literature
UnknownMulti-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.
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S-EPMC12330429 | biostudies-literature
UnknownLipoprotein(a) and Benefit of PCSK9 Inhibition in Patients With Nominally Controlled LDL Cholesterol.
Not available
S-EPMC8822604 | biostudies-literature
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