Minimum birth prevalence of mitochondrial respiratory chain disorders in children
- Author
- SKLADAL, Daniela1 2 ; HALLIDAY, Jane1 3 ; THORBURN, David R1 4 5
[1] The Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia
[2] Children's Hospital, Innsbruck, Austria
[3] Birth Defects Register, Public Health Division, Department of Human Services, Melbourne, Australia
[4] Genetic Health Services Victoria, Royal Children's Hospital, Melbourne, Australia
[5] Department of Paediatrics, University of Melbourne, Melbourne, Australia - Source
Brain. 2003, Vol 126, pp 1905-1912, 8 p ; 8 ; ref : 26 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Cytopathie mitochondriale Enfant Etude statistique Naissance Prévalence Enzymopathie Homme Maladie héréditaire Métabolisme pathologie
- Keyword (en)
- Mitochondrial disorder Child Statistical study Birth Prevalence Enzymopathy Human Genetic disease Metabolic diseases
- Keyword (es)
- Citopatía mitocondrial Niño Estudio estadístico Nacimiento Prevalencia Enzimopatía Hombre Enfermedad hereditaria Metabolismo patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D05 Miscellaneous hereditary metabolic disorders
- Discipline
- Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 14993309
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
10.1093/brain/awg170 
https://dx.doi.org/10.1093/brain/awg170
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