QuickView for CCDC88C (gene)

1. A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic parapl…
2. Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants.
3. Beneficial tyrosine kinase inhibitor therapy in a patient with relapsed BCR-ABL1-like acute lymphobl…
4. Two Isoforms of the Guanine Nucleotide Exchange Factor, Daple/CCDC88C Cooperate as Tumor Suppressors…
5. CCDC88C-FLT3 gene fusion in CD34-positive haematopoietic stem and multilineage cells in myeloid/lymp…

There were no clinical trials for CCDC88C