A tRNALys mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome
- Author
- NOER, A. S1 ; SUDOYO, H; LERTRIT, P; THYAGARAJAN, D; UTTHANAPHOL, P; KAPSA, R; BYRNE, E; MARZUKI, S
[1] Monash univ., cent. molecular biology medicine, dep. biochemistry, Clayton, Victoria 3168, Australia - Source
American journal of human genetics. 1991, Vol 49, Num 4, pp 715-722 ; ref : 1 p
- Publisher
- University of Chicago Press, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Epilepsie Exploration Génétique Mutation Myoclonie Système nerveux pathologie Encéphalomyopathie mitochondriale MERRF syndrome
- Keyword (en)
- Epilepsy Exploration Genetics Mutation Myoclonus Nervous system diseases
- Keyword (es)
- Epilepsia Exploración Genética Mutación Mioclonia Sistema nervioso patología
- Classification
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5295664
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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