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Bifunctional enzyme deficiency: Identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal β‐oxidation of unknown aetiology by means of complementation analysis
Author(s) -
Wanders R. J. A.,
Roermund C. W. T.,
Brul S.,
Schutgens R. B. H.,
Tager J. M.
Publication year - 1992
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/bf02435983
Subject(s) - peroxisomal disorder , etiology , university hospital , medicine , pediatrics , peroxisome , family medicine , receptor
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