QuickView for CC2D2A, N-terminal, C2 domain (biogroup)

1. OMIM - Joubert and Meckel syndromes
2. Peripheral blood of convalescent mild/moderate & severe/critical COVID-19 individuals
3. OMIM - COACH syndrome
4. Caenorhabditis elegans xpa-1 deletion mutants [OK698]
5. Caenorhabditis elegans gene expression in nth-1 and xpa-1 mutants deficient in DNA repair

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There were no clinical trials for CC2D2A, N-terminal, C2 domain