QuickView for ZNF592;jsessionid=2786B5B749A1BDE3323CC1771ABF36AF (gene)

1. Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients.
2. CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zi…
3. Misleading Germ Cell Phenotype in Pulmonary NUT Carcinoma Harboring the ZNF532-NUTM1 Fusion.
4. Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strat…
5. Investigation of de novo unique differentially expressed genes related to evolution in exercise resp…

There were no clinical trials for ZNF592;jsessionid=2786B5B749A1BDE3323CC1771ABF36AF