QuickView for rnf216 protein human (compound)

No studies found

1. Clinical and genetic spectrum of RNF216-related disorder: a new case and literature review.
2. Ring finger protein 216 loss-of-function induces white matter hyperintensities by inhibiting oligode…
3. Establishment of FDHSi003-A, a human induced pluripotent stem cell (hiPSC) line with a mutation of R…
4. Whole-Exome Sequencing Identified a Novel Mutation in RNF216 in a Family with Gordon Holmes Syndrome…
5. A novel mutation in RNF216 gene in an Indian case with Gordon Holmes syndrome.

There were no clinical trials for rnf216 protein human