Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
- Author
- HANEFELD, F. A; ERNST, B. P; WILICHOWSKI, E; CHRISTEN, H.-J
Univ. Göttingen, dep. pediatrics neuropediatrics, Göttingen 37075, Germany - Source
Neuropediatrics. 1994, Vol 25, Num 6 ; p. 331 ; ref : 4 ref
- CODEN
- NRPDDB
- ISSN
- 0174-304X
- Scientific domain
- Neurology; Pediatrics
- Publisher
- Thieme, Stuttgart
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- DNA Dégénérescence neurorétinienne héréditaire Leber Exploration Homme Mitochondrie Mutation Sclérose en plaque Maladie héréditaire Maladie inflammatoire Oeil pathologie Rétinopathie Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- DNA Leber amaurosis Exploration Human Mitochondria Mutation Multiple sclerosis Genetic disease Inflammatory disease Eye disease Retinopathy Central nervous system disease Nervous system diseases
- Keyword (es)
- DNA Degeneración neuroretiniana hereditaria Leber Exploración Hombre Mitocondria Mutación Esclerosis en placa Enfermedad hereditaria Enfermedad inflamatoria Ojo patología Retinopatía Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17F Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3417042
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
10.1055/s-2008-1073049 
https://dx.doi.org/10.1055/s-2008-1073049
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