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Systemic carnitine deficiency due to lack of electron transfer flavoprotein: ubiquinone oxidoreductase

Author
DI DONATO, S1 ; FRERMAN, F. E; RIMOLDI, M; RINALDO, P; TARONI, F; WIESMANN, U. N
[1] Ist. neurologico C. Besta, Milan 20133, Italy
Source

Neurology. 1986, Vol 36, Num 7, pp 957-963 ; ref : 31 ref

CODEN
NEURAI
ISSN
0028-3878
Scientific domain
Neurology
Publisher
Lippincott Williams & Wilkins, Hagerstown, MD
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Acidurie glutarique II Carence vitaminique Carnitine Déficit Enfant Flavoprotéine Lipide Maladie héréditaire Métabolisme pathologie Transfert électron Ubiquinol-cytochrome c reductase Homme
Keyword (en)
Glutaric aciduria II Vitamin deficiency Carnitine Deficiency Child Flavoprotein Lipids Genetic disease Metabolic diseases Electron transfer Ubiquinol-cytochrome c reductase Human
Keyword (es)
Carencia vitaminica Deficit Niño Flavoproteina Lipido Enfermedad hereditaria Metabolismo patologia Transferencia electron Hombre
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
7999726

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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