ParkinsonFranceV1, Ncbi, Curation, indexItem, KwdEn.i, Mutation

Mutant Proteins (metabolism) < Mutation < Mutation (genetics)

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 42.
[0-20] [0 - 20][0 - 42][20-40]**** probable Xml problem ****

Ident.	Authors (with country if any)	Title
000007 (1999)	N. Abbas [France] ; C B Lücking ; S. Ricard ; A. Dürr ; V. Bonifati ; G. De Michele ; S. Bouley ; J R Vaughan ; T. Gasser ; R. Marconi ; E. Broussolle ; C. Brefel-Courbon ; B S Harhangi ; B A Oostra ; E. Fabrizio ; G A Böhme ; L. Pradier ; N W Wood ; A. Filla ; G. Meco ; P. Denefle ; Yves Agid [France] ; A. Brice	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
000040 (1999)	M B Delisle [France] ; J R Murrell ; R. Richardson ; J A Trofatter ; O. Rascol ; X. Soulages ; M. Mohr ; P. Calvas ; B. Ghetti	A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.
000117 (2000)	C A Da Costa [France] ; K. Ancolio ; F. Checler	Wild-type but not Parkinson's disease-related ala-53 --> Thr mutant alpha -synuclein protects neuronal cells from apoptotic stimuli.
000153 (2000)	M. Farrer [États-Unis] ; T. Destée ; E. Becquet ; F. Wavrant-De Vrièze ; V. Mouroux ; F. Richard ; L. Defebvre ; S. Lincoln ; J. Hardy ; P. Amouyel ; M C Chartier-Harlin	Linkage exclusion in French families with probable Parkinson' s disease.
000165