Associated Papers
Whole-Exome Sequencing Reveals Novel Candidate Driver Mutations and Potential Druggable Mutations in Patients with High-Risk Neuroblastoma.
Nokchan N et al.
Journal of Personalized Medicine, 2024
39338204 (PubMed )
Supplement: jpm-14-00950-s001.zip › Supplementary_Table_S4.xlsx › Supplementary_Table_S4.
Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.
Cai R et al.
Frontiers in Cell and Developmental Biology, 2021
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