A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
- Author
- ABBAS, N1 ; LÜCKING, C. B1 ; BROUSSOLLE, E8 ; BREFEL-COURBON, C9 ; HARHANGI, B. S10 ; OOSTRA, B. A11 ; FABRIZIO, E2 ; BÖHME, G. A12 ; PRADIER, L12 ; WOOD, N. W5 ; FILLA, A3 ; MECO, G2 ; RICARD, S1 ; DENEFLE, P4 ; AGID, Y1 ; BRICE, A1 ; DÜRR, A1 ; BONIFATI, V2 ; DE MICHELE, G3 ; BOULEY, S4 ; VAUGHAN, J. R5 ; GASSER, T6 ; MARCONI, R7
[1] INSERM U289, Hôpital de la Salpêtrière, 47 Boulevard de l'Hôpital, 75651 Paris, France
[2] Dipartimento di Scienze Neurologiche, Università ' La Sapienza', 00185 Rome, Italy
[3] Dipartimento di Scienze Neurologiche, Università Federico II, 80131 Naples, Italy
[4] Genomics Department, Rhone-Poulenc Rorer, 91006 Evry, France
[5] Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom
[6] Neurologische Klinik, Klinikum Grosshadern, Ludwig-Maximilians-Universität, 81377 Munich, Germany
[7] Divisione di Neurologia, Ospedale Misericordia, 58100 Grosseto, Italy
[8] Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, 69003 Lyon, France
[9] Service de Pharmacologie-Centre d'lnvestigation Clinique, INSERM U455, CHU de Toulouse, 31073 Toulouse, France
[10] Department of Epidemiology and Biostatistics, Erasmus University Medical School, 3000 DR Rotterdam, Netherlands
[11] Department of Clinical Genetics, Erasmus University, 3015 GE Rotterdam, Netherlands
[12] CNS Department, Rhone-Poulenc Rorer, 94400 Vitry, France
European Consortium on Genetic Susceptibility in Parkinson's Disease, Europe - Source
Human molecular genetics (Print). 1999, Vol 8, Num 4, pp 567-574 ; ref : 19 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Caractère autosomique Caractère récessif Chromosome C6 Etude familiale Génétique Homme Mutation Parkinson maladie Polymorphisme Gène parkin Europe Encéphale pathologie Extrapyramidal syndrome Maladie dégénérative Maladie héréditaire Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Autosomal character Recessive character Chromosome C6 Family study Genetics Human Mutation Parkinson disease Polymorphism Europe Cerebral disorder Extrapyramidal syndrome Degenerative disease Genetic disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Carácter autosómico Carácter recesivo Cromosoma C6 Estudio familiar Genética Hombre Mutación Parkinson enfermedad Polimorfismo Europa Encéfalo patología Extrapiramidal síndrome Enfermedad degenerativa Enfermedad hereditaria Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution / 002A07C Classical genetics, quantitative genetics, hybrids / 002A07C03 Human
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1742625
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1093/hmg/8.4.567 
https://dx.doi.org/10.1093/hmg/8.4.567
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