QuickView for ARCN1;jsessionid=D05119E401BD3D095815864D73D2BF43 (gene)

1. The Radiological and Histological Phenotype of Skeletal Abnormalities in Fetal ARCN1-Related Syndrom…
2. Expanding the phenotypic spectrum of ARCN1-related syndrome.
3. MicroRNA-33a disturbs influenza A virus replication by targeting ARCN1 and inhibiting viral ribonucl…
4. ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects.
5. δ-COP contains a helix C-terminal to its longin domain key to COPI dynamics and function.

There were no clinical trials for ARCN1;jsessionid=D05119E401BD3D095815864D73D2BF43