Associated Papers
Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry.
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Journal of Molecular Medicine (berlin, Germany), 2025
39730912 (PubMed )
Supplement: 109_2024_2510_MOESM2_ESM.xlsx › Sheet1
Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder.
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Annals of Clinical and Translational Neurology, 2020
32105419 (PubMed )
Supplement: ACN3-7-390-s001.docx
Patient-derived glioblastoma organoids reflect tumor heterogeneity and treatment sensitivity.
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Supplement: vdad152_suppl_supplementary_materials_5.xlsx › SNVs
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