Associated Papers
Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly.
Gross A et al.
Febs Letters, 2024
Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability.
Hu J et al.
Genes, 2022
35627197 (PubMed )
Supplement: genes-13-00813-s001.zip › genes-1688186-supplementary › Supplementary_Table_S1-final.xlsx › Sheet2
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