Associated Papers
Understanding rare variant contributions to autism: lessons from dystrophin-deficient model.
Costa CIS et al.
Npj Genomic Medicine, 2025
40050609 (PubMed )
Supplement: 41525_2025_469_MOESM1_ESM.pdf
Identification of heritable rare variants associated with early-stage lung adenocarcinoma risk.
Fu R et al.
Translational Lung Cancer Research, 2022
Select a paper to view details