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The Journal of Cell Biology|April 21, 2010
Regulation of exosome secretion by Rab35 and its GTPase-activating proteins TBC1D10A-CChieh Hsu, Yuichi Morohashi, Shin-Ichiro Yoshimura, et al.Open Biology|September 15, 2012
Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancerRavi K Nookala, Lars Langemeyer, Angela Pacitto, et al.American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.Nature Genetics|November 11, 2008
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golginHans Christian Hennies, Uwe Kornak, Haikuo Zhang, et al.American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.American Journal of Human Genetics|April 9, 2011
Loss-of-function mutations in RAB18 cause Warburg micro syndromeDanai Bem, Shin-Ichiro Yoshimura, Ricardo Nunes-Bastos, et al.Pageof 10