Journal article

Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with alpha-Synuclein Pathology

Gabrielle R Wilson, Joe CH Sim, Catriona McLean, Maila Giannandrea, Charles A Galea, Jessica R Riseley, Sarah EM Stephenson, Elizabeth Fitzpatrick, Stefan A Haas, Kate Pope, Kirk J Hogan, Ronald G Gregg, Catherine J Bromhead, David S Wargowski, Christopher H Lawrence, Paul A James, Andrew Churchyard, Yujing Gao, Dean G Phelan, Greta Gillies Show all

The American Journal of Human Genetics | CELL PRESS | Published : 2014


Awarded by Australian National Health and Medical Research Council (NHMRC)

Awarded by NHMRC

Awarded by Parkinson's Disease Foundation

Awarded by GENCODYS by European Union

Awarded by Australian Research Council Future Fellowship

Funding Acknowledgements

We thank the families for their participation in this study and the generous support of the Lefroy and Handbury families. This work was funded in part by Australian National Health and Medical Research Council (NHMRC) program grant 490037 to D.J.A. and M.B., NHMRC project grant APP1041860 to P.J.L., Parkinson's Disease Foundation grant PDF-IRG-1220 to P.J.L. and G.R.W., and the project GENCODYS (grant 241995 to V.M.K.), which was funded by the European Union Framework Programme 7. P.J.L. was supported by an NHMRC Career Development Fellowship (APP1032364), and M.B. was supported by an Australian Research Council Future Fellowship (FT100100764). This work was made possible through Victorian State Government Operational Infrastructure Support and the NHMRC Independent Medical Research Institutes Infrastructure Support Scheme.