T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson disease
- Author
- CHISHTI, Muhammad A1 ; BOHLEGA, Saeed2 ; AHMED, Maqbool1 ; LOUALICH, Arslan1 ; CARROLL, Pamela3 ; SATO, Christine4 ; ST GEORGE-HYSLOP, Peter4 5 ; WESTAWAY, David4 ; ROGAEVA, Ekaterina4
[1] Department of Comparative Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
[2] Department of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
[3] Department of Aragene Laboratory, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
[4] Centre for Research in Neurodegenerative Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada
[5] Toronto Western Hospital Research Institute, University of Toronto, Toronto, Ontario, Canada - Source
Archives of neurology (Chicago). 2006, Vol 63, Num 10, pp 1483-1485, 3 p ; ref : 15 ref
- Publisher
- American Medical Association, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Mutation Parkinson maladie Système nerveux pathologie Encéphale pathologie Extrapyramidal syndrome Maladie dégénérative Système nerveux central pathologie
- Keyword (en)
- Mutation Parkinson disease Nervous system diseases Cerebral disorder Extrapyramidal syndrome Degenerative disease Central nervous system disease
- Keyword (es)
- Mutación Parkinson enfermedad Sistema nervioso patología Encéfalo patología Extrapiramidal síndrome Enfermedad degenerativa Sistema nervosio central patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A03 Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
- 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
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18209255
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
10.1001/archneur.63.10.1483 
https://dx.doi.org/10.1001/archneur.63.10.1483
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