Associated Papers
The Biology of tRNA t6A Modification and Hypermodifications-Biogenesis and Disease Relevance.
Zhang W et al.
Journal of Molecular Biology, 2025
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
Barbosa P et al.
Frontiers in Cardiovascular Medicine, 2022
36061567 (PubMed )
Supplement: Table_1.XLSX › Table_S6
Biallelic variants in YRDC cause a developmental disorder with progeroid features.
Schmidt J et al.
Human Genetics, 2021
Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome.
Arrondel C et al.
Nature Communications, 2019
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