Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy
- Author
- MINASSIAN, B. A1 2 3 4 ; SAINZ, J1 2 ; CARPENTER, S10 ; WIGG, K10 8 ; SANGHVI, A. V1 ; DELGADO-ESCUETA, A. V1 11 2 ; SERRATOSA, J. M1 2 5 ; GEE, M1 2 ; SAKAMOTO, L. M1 2 ; BOHLEGA, S6 ; GEOFFROY, G7 ; BARR, C4 8 ; SCHERER, S. W4 ; TOMIYASU, U9
[1] Comprehensive Epilepsy Program, Department of Neurology, University of California, Los Angeles. CA, United States
[2] Neurology and Research Service, West Los Angeles DVA Medical Center, Los Angeles. CA, United States
[3] Division of Neurology, Department of Pediatrics, Bloorview Epilepsy Program, Toronto, Ontario, United States
[4] Department of Genetics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, United States
[5] Epilepsy Unit, Jimenez Diaz Foundation, Madrid, Spain
[6] Department of Medicine, King Faisal Specialist Hospital, Riyadh, Saudi Arabia
[7] Department of Neurology, Ste-Justine Hospital, University of Montreal, Montreal, Canada
[8] Department of Psychiatry, The Toronto Hospital, University of Toronto, Toronto, Ontario, Canada
[9] Pathology Services, West Los Angeles DVA Medical Center, Los Angeles. CA, United States
[10] Department of Pathology, The Toronto Hospital, University of Toronto, Toronto, Ontario, Canada
[11] Brain Research Institute, University of California, Los Angeles School of Medicine, Los Angeles. CA, United States - Source
Annals of neurology. 1999, Vol 45, Num 2, pp 262-265 ; ref : 19 ref
- Publisher
- Willey-Liss, Hoboken
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Corps Lafora Epilepsie myoclonique familiale Unverricht Lundborg Etude familiale Exploration Homme Hétérogénéité Locus Encéphale pathologie Maladie dégénérative Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Lafora body Progressive myoclonus epilepsy Family study Exploration Human Heterogeneity Locus Cerebral disorder Degenerative disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Cuerpos Lafora Epilepsia mioclónica progresiva Estudio familiar Exploración Hombre Heterogeneidad Locus Encéfalo patología Enfermedad degenerativa 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
- 1676181
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
10.1002/1531-8249(199902)45:2<262::AID-ANA20>3.0.CO;2-9 
https://dx.doi.org/10.1002/1531-8249(199902)45:2<262::AID-ANA20>3.0.CO;2-9
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