Associated Papers
Molecular characterization of recessively inherited ataxic and neuropathic disorders in consanguineous Pakistani families.
Aslam F et al.
Scientific Reports, 2026
41606223 (PubMed )
Supplement: 41598_2026_37808_MOESM3_ESM.xlsx › Sheet1
Identification of ZBTB24 protein domains and motifs for heterochromatin localization and transcriptional activation.
Aktar S et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms, 2019
A functional assay to classify ZBTB24 missense variants of unknown significance.
Wu H et al.
Human Mutation, 2019
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