Associated Papers
The Biology of tRNA t6A Modification and Hypermodifications-Biogenesis and Disease Relevance.
Zhang W et al.
Journal of Molecular Biology, 2025
Novel TP53RK variants cause varied clinical features of Galloway-Mowat syndrome without nephrotic syndrome in three unrelated Chinese patients.
Chen J et al.
Frontiers in Molecular Neuroscience, 2023
Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome.
Treimer E et al.
Human Mutation, 2022
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