Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease With α-Synuclein Pathology.
Wilson GR, Sim JC, McLean C, Giannandrea M, Galea CA, Riseley JR, Stephenson SE, Fitzpatrick E, Haas SA, Pope K, Hogan KJ, Gregg RG, Bromhead CJ, Wargowski DS, et al. (2014). Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. American Journal of Human Genetics, 95(6):729-35. doi: 10.1016/j.ajhg.2014.10.015.