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

Pneumonia, Aspiration (prevention & control) < Point Mutation < Point Mutation (genetics)

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List of bibliographic references

Number of relevant bibliographic references: 9. **** 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.
000017 (1999)	S S Mirra [États-Unis] ; J R Murrell ; M. Gearing ; M G Spillantini ; M. Goedert ; R A Crowther ; A I Levey ; R. Jones ; J. Green ; J M Shoffner ; B H Wainer ; M L Schmidt ; J Q Trojanowski ; B. Ghetti	Tau pathology in a family with dementia and a P301L mutation in tau.
000054 (1999)	B S Harhangi [Pays-Bas] ; M J Farrer ; S. Lincoln ; V. Bonifati ; G. Meco ; G. De Michele ; A. Brice ; A. Dürr ; M. Martinez ; T. Gasser ; B. Bereznai ; J R Vaughan ; N W Wood ; J. Hardy ; B A Oostra ; M M Breteler	The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
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