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Zellweger‐like phenotype in two siblings: A defect in peroxisomal β‐oxidation with elevated very long‐chain fatty acids but normal bile acids
Author(s) -
Mandel H.,
Berant M.,
Aizin A.,
Gershony R.,
Hemmli S.,
Schutgens R. B. H.,
Wanders R. J. A.
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/bf02435982
Subject(s) - peroxisomal disorder , center (category theory) , medical school , medicine , peroxisome , pediatrics , chemistry , medical education , receptor , crystallography