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Mitochondrial respiratory chain disorders I : mitochondrial DNA defects

Author
LEONARD, J. V1 ; SCHAPIRA, A. H. V2
[1] Biochemistry, Endocrine and Metabolic Unit, Institute of Child Health, London, United Kingdom
[2] University Department of Clinical Neurosclences, Royal Free and University College Medical School, and Institute of Neurology, University College London, London, United Kingdom
Source

Lancet (British edition). 2000, Vol 355, Num 9200, pp 299-304 ; ref : 34 ref

CODEN
LANCAO
ISSN
0140-6736
Scientific domain
General medicine general surgery
Publisher
Lancet, London
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
ATP Article synthèse Biologie moléculaire Cellule Cytopathie mitochondriale DNA Génétique Homme Métabolisme Phosphorylation oxydative Transport biologique Enzymopathie Maladie héréditaire Métabolisme pathologie
Keyword (en)
ATP Review Molecular biology Cell Mitochondrial disorder DNA Genetics Human Metabolism Oxidative phosphorylation Biological transport Enzymopathy Genetic disease Metabolic diseases
Keyword (es)
ATP Artículo síntesis Biología molecular Célula Citopatía mitocondrial DNA Genética Hombre Metabolismo Fosforilación oxidativa Transporte biológico Enzimopatía Enfermedad hereditaria Metabolismo patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D02 Lipids (lysosomal enzyme disorders, storage diseases)

Discipline
Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1260191

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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