QuickView for DMSA;jsessionid=B2D1EB755E1133E744B4718A2FA4249F;jsessionid=6AC2512ECA6FAF4390D167931DBF4136;jsessionid=F6FBCF83893029FB8A0F0B972E61E7B0;jsessionid=FE77C38C24B7710D0D62559D790590DC (gene)

1. Novel STAG1 Frameshift Mutation in a Patient Affected by a Syndromic Form of Neurodevelopmental Diso…
2. ML-SA1 and SN-2 inhibit endocytosed viruses through regulating TRPML channel expression and activity…
3. Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies.
4. Cohesinopathy presenting with microtia, facial palsy, and hearing loss caused by STAG1 pathogenic va…
5. STAG1 vulnerabilities for exploiting cohesin synthetic lethality in STAG2-deficient cancers.

There were no clinical trials for DMSA;jsessionid=B2D1EB755E1133E744B4718A2FA4249F;jsessionid=6AC2512ECA6FAF4390D167931DBF4136;jsessionid=F6FBCF83893029FB8A0F0B972E61E7B0;jsessionid=FE77C38C24B7710D0D62559D790590DC