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1. Coupling fission and exit of RAB6 vesicles at Golgi hotspots through kinesin-myosin interactions. Issue 1 (December 2017)

2. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Issue 3 (17th January 2018)