Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: Detailed genetic mapping of the linked region

Author

JONES, A. C¹ ; YAMAMURA, Y² ; NYGAARD, T. G¹ ; ALMASY, L^{1 3} ; BOHLEGA, S⁴ ; ELIBOL, E⁵ ; HUBBLE, J⁶ ; KUZUHARA, S⁷ ; UCHIDA, M⁸ ; YANAGI, T⁹ ; WEEKS, D. E^{10 11 12}
[1] Department of Neurology, Columbia University College of Physicians and Surgeons, New York, United States
[2] Institute of Health Sciences, Hiroshima, Japan
[3] University School of Medicine, Hiroshima, Japan
[4] Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, United States
[5] Department of Neurology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
[6] Department of Neurology, Hacettepe University Hospitals, Sihhiye, Ankara, Turkey
[7] Department of Neurology, Ohio State University Hospitals, Columbus, United States
[8] Department of Neurology, Mie University School of Medicine, Tsu City, Japan
[9] Tosei General Hospital, Seto City, Japan
[10] Second Nagoya Red Cross Hospital, Nagoya City, Japan
[11] Department of Genetics, University of Pittsburgh, Pittsburgh, United States
[12] The Wellcome Trust Centre for Human Genetics, Oxford, United States

Source

American journal of human genetics. 1998, Vol 63, Num 1, pp 80-87 ; ref : 1 p.1/4

CODEN

AJHGAG

ISSN

0002-9297

Scientific domain

Genetics

Publisher

University of Chicago Press, Chicago, IL

Publication country

United States

Document type

Article

Language

English

Keyword (fr)

Caractère autosomique Caractère récessif Carte génétique Chromosome C6 Déterminisme génétique Ethnie Etude familiale Gène Homme Liaison génétique Locus Parkinson maladie Superoxide dismutase Encéphale pathologie Enzyme Extrapyramidal syndrome Maladie dégénérative Maladie héréditaire Oxidoreductases Système nerveux central pathologie Système nerveux pathologie

Keyword (en)

Autosomal character Recessive character Genetic mapping Chromosome C6 Genetic determinism Ethnic group Family study Gene Human Linkage Locus Parkinson disease Superoxide dismutase Cerebral disorder Enzyme Extrapyramidal syndrome Degenerative disease Genetic disease Oxidoreductases Central nervous system disease Nervous system diseases

Keyword (es)

Carácter autosómico Carácter recesivo Mapa genético Cromosoma C6 Determinismo genético Etnia Estudio familiar Gen Hombre Ligamiento genético Locus Parkinson enfermedad Superoxide dismutase Encéfalo patología Enzima Extrapiramidal síndrome Enfermedad degenerativa Enfermedad hereditaria Oxidoreductases Sistema nervosio central patología Sistema nervioso patología

Classification

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

2312461

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