QuickView for rabenosyn-5 (gene)

1. Identification of New Interactions between Endolysosomal Tethering Factors.
2. Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN.
3. Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective…
4. FERARI is required for Rab11-dependent endocytic recycling.
5. RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, …

There were no clinical trials for rabenosyn-5