A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
- Author
- KAMINEN, N1 ; HANNULA-JOUPPI, K1 ; KERE, J1 7 ; KESTILÄ, M2 ; LAHERMO, P3 ; MULLER, K4 ; KAARANEN, M4 ; MYLLYLUOMA, B5 ; VOUTILAINEN, A5 ; LYYTINEN, H4 ; NOPOLA-HEMMI, J1 5 6
[1] Department of Medical Genetics, Biomedicum, University of Helsinki, Finland
[2] Department of Molecular Medicine, National Public Health Institute, Biomedicum, Helsinki, Finland
[3] Finnish Genome Centre, University of Helsinki, Finland
[4] Department of Psychology and Child Research Centre, University of Jyväskylä, Finland
[5] Department of Paediatric Neurology, Hospital for Children and Adolescents, University of Helsinki, Finland
[6] Department of Paediatrics, Jorvi Hospital, Espoo, Finland
[7] Department of Biosciences at Novum and Clinical Research Centre, Karolinska Institute, Sweden - Source
Journal of medical genetics. 2003, Vol 40, Num 5, pp 340-345, 6 p ; ref : 37 ref
- Publisher
- BMJ, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Chromosome A2 Chromosome C7 Chromosome Dyslexie Déterminisme génétique Génome Homme Liaison génétique Locus Pathogénie Génétique Système nerveux pathologie Trouble communication Trouble langage Trouble lecture Trouble neurologique
- Keyword (en)
- Chromosome A2 Chromosome C7 Chromosome Dyslexia Genetic determinism Genome Human Linkage Locus Pathogenesis Genetics Nervous system diseases Communication disorder Language disorder Reading disorder Neurological disorder
- Keyword (es)
- Cromosoma A2 Cromosoma C7 Cromosoma Dislexia Determinismo genético Genoma Hombre Ligamiento genético Locus Patogenia Genética Sistema nervioso patología Trastorno comunicación Trastorno lenguaje Trastorno lectura Trastorno neurológico
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A02 Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 14804260
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
10.1136/jmg.40.5.340 
https://dx.doi.org/10.1136/jmg.40.5.340
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