QuickView for CCDC115;jsessionid=200B78EB20321950392834B4BC960FB5 (gene)

1. Defective Lipid Droplet-Lysosome Interaction Causes Fatty Liver Disease as Evidenced by Human Mutati…
2. Genetic screens reveal CCDC115 as a modulator of erythroid iron and heme trafficking.
3. Distinct roles of α- and β-tubulin polyglutamylation in controlling axonal transport and in neurodeg…
4. The vacuolar-ATPase complex and assembly factors, TMEM199 and CCDC115, control HIF1α prolyl hydroxyl…
5. Genetics of Wilson disease and Wilson-like phenotype in a clinical series from eastern Spain.

There were no clinical trials for CCDC115;jsessionid=200B78EB20321950392834B4BC960FB5