Associated Papers
De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.
Liang XY et al.
Epilepsia, 2025
De novo genic mutations among a Chinese autism spectrum disorder cohort.
Wang T et al.
Nature Communications, 2016
27824329 (PubMed )
Supplement: ncomms13316-s7.xlsx › Supplementary_Data_6
Select a paper to view details