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NADH:Q 1 oxidoreductase deficiency without lactic acidosis in a patient with leigh syndrome: Implications for the diagnosis of inborn errors of the respiratory chain
Author(s) -
Wijburg F. A.,
Wanders R. J. A.,
Lie Peters E. M.,
Vos G. D.,
Loggers H. G.,
Bolhuis P. A.,
Herzberg N. H.,
Ruitenbeek W.,
Wilsem A.,
Houten R.,
Barth P. G.
Publication year - 1991
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01811686
Subject(s) - university hospital , pediatrics , medicine , emergency department , neurology , pediatric neurology , emergency medicine , psychiatry