QuickView for POLR3A;jsessionid=DDCADFBEC260FAF19545B625B663F2B8 (gene)

1. Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A.
2. Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 c…
3. An iPSC model for POLR3A-associated spastic ataxia: Generation of three unrelated patient cell lines…
4. A novel variant of the POLR3A gene in a Chinese patient with POLR3-related leukodystrophy.
5. DNA from macrophages induces fibrosis and vasculopathy through POLR3A/STING/type I interferon axis i…

There were no clinical trials for POLR3A;jsessionid=DDCADFBEC260FAF19545B625B663F2B8