Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndrome
- Author
- JOHNS, D. R; THRELKELD, A. B; MILLER, N. R; HURKO, O
Johns Hopkins univ. school medicine, dep. neurology, United States - Source
American journal of ophthalmology. 1993, Vol 115, Num 1, pp 108-109 ; ref : 5 ref
- CODEN
- AJOPAA
- ISSN
- 0002-9394
- Scientific domain
- Ophthalmology
- Publisher
- Elsevier, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Adulte DNA mitochondrial Délétion Encéphalopathie Etude cas Génétique Myoneurogastrointestinal encéphalopathie syndrome Système nerveux central pathologie Aberration chromosomique Appareil digestif pathologie Chromosome anormal Encéphale pathologie Homme Muscle strié pathologie Système nerveux pathologie
- Keyword (en)
- Adult Mitochondrial DNA Deletion Encephalopathy Case study Genetics Chromosomal aberration Digestive diseases Abnormal chromosome Cerebral disorder Human Striated muscle disease Nervous system diseases
- Keyword (es)
- Adulto DNA mitocondrial Deleción Encefalopatía Estudio caso Genética Aberración cromosómica Aparato digestivo patología Cromosoma anormal Encéfalo patología Hombre Músculo estriado patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4516255
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
10.1016/S0002-9394(14)73533-0 
https://dx.doi.org/10.1016/S0002-9394(14)73533-0
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