Associated Papers
WDR26-related Skraban-Deardorff syndrome: clinical, genetic and pathomechanistic insights.
Lin X et al.
European Journal of Medical Research, 2025
40826479 (PubMed )
Supplement: 40001_2025_3024_MOESM2_ESM.xlsx › Sheet1
Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly.
Gross A et al.
Febs Letters, 2024
38575527 (PubMed )
Supplement: EMS198546-supplement-Supplemental_material.pdf
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
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM10_ESM.xlsx › Supplementary_Data_8
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