M. C. Chartier-harlin, J. C. Dachsel, C. Vilarino-guell, S. J. Lincoln, F. Lepretre et al., Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease, The American Journal of Human Genetics, vol.89, issue.3, pp.398-406, 2011.
DOI : 10.1016/j.ajhg.2011.08.009

O. Corti, S. Lesage, and A. Brice, What Genetics Tells us About the Causes and Mechanisms of Parkinson's Disease, Physiological Reviews, vol.91, issue.4, pp.1161-1218, 2011.
DOI : 10.1152/physrev.00022.2010

A. J. Hughes, S. E. Daniel, L. Kilford, and A. J. Lees, Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases., Journal of Neurology, Neurosurgery & Psychiatry, vol.55, issue.3, pp.181-184, 1992.
DOI : 10.1136/jnnp.55.3.181

S. Lesage, C. Condroyer, A. Lannuzel, E. Lohmann, A. Troiano et al., Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease, Journal of Medical Genetics, vol.46, issue.7, pp.458-464, 2009.
DOI : 10.1136/jmg.2008.062612

O. A. Ross, A. I. Soto-ortolaza, M. G. Heckman, J. O. Aasly, N. Abahuni et al., Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case???control study, The Lancet Neurology, vol.10, issue.10, pp.898-908, 2011.
DOI : 10.1016/S1474-4422(11)70175-2

J. Wszolek, Z. K. Vingerhoets, F. Farrer, and M. J. , VPS35 mutations in Parkinson disease, Am. J. Hum. Genet, vol.89, pp.162-167, 2011.

A. Zimprich, A. Benet-pages, W. Struhal, E. Graf, S. H. Eck et al., A mutation in VPS35, pp.12-215, 2011.