Associated Papers
MED13L-related disorder characterized by severe motor speech impairment.
Mitchel MW et al.
Journal of Neurodevelopmental Disorders, 2025
40993520 (PubMed )
Supplement: 11689_2025_9645_MOESM1_ESM.xlsx › Table_S2
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou X et al.
Nature Genetics, 2022
35982159 (PubMed )
Supplement: 41588_2022_1148_MOESM6_ESM.xlsx › SupplementaryData2_ASD_Rep_DNVs
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Zhang Y et al.
Molecular Neurobiology, 2021
33860439 (PubMed )
Supplement: 12035_2021_2377_MOESM10_ESM.xlsx › Sheet1
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