Muscle strength in children with medium‐chain acyl‐CoA dehydrogenase deficiency

Saved in:
Bibliographic Details
Published inJournal of inherited metabolic disease Vol. 22; no. 2; pp. 200 - 201
Main Authors Custers, J. W. H., Poll‐The, B. T., Duran, M., Klerk, J. B. C., Uiterwaal, C. S. P. M., Helders, P. J. M.
Format Journal Article
LanguageEnglish
Published Dordrecht Kluwer Academic Publishers 01.04.1999
Springer
Blackwell Publishing Ltd
Subjects
Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenases - deficiency
Adolescent
Biological and medical sciences
Child
Errors of metabolism
Female
Humans
Lipid Metabolism, Inborn Errors - physiopathology
Lipids (lysosomal enzyme disorders, storage diseases)
Male
Medical sciences
Metabolic diseases
Muscle Weakness - enzymology
Muscle Weakness - physiopathology
Retrospective Studies
Human
Hypolipemia
Enzyme
Deficiency
Metabolic diseases
Lipids
Enzymopathy
Muscle contraction
Acyl-CoA dehydrogenase
Genetic disease
Clinical investigation
Oxidoreductases
Child
Online AccessGet full text

Cover

More Information
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0141-8955
1573-2665
DOI:10.1023/A:1005491128746