Characteristic urine organic acid profile in peroxisomal biogenesis disorders
Author:
Affiliation:
1. ; Department of Clinical Biochemistry; Hadassah University Hospital; Jerusalem Israel
2. ; Department of Pediatrics B; Rambam Medical Center; Haifa Israel
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005624523611/fullpdf
Reference9 articles.
1. Clinical approach to inherited peroxisomal disorders: a series of 27 patients;Baumgartner;Ann Neurol,1998
2. Azelaic and pimelic acids: metabolic intermediates or artefacts?;Bennett;J Inherit Metab Dis,1992
3. Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome-importance of peroxisomes in b-oxidation of dicarboxylic acids;Björkhem;Biochim Biophys Acta,1984
4. Excretion of 3,6-epoxydicarboxylic acids in peroxisomal disorders;Pitt;Clin Chim Acta,1993
5. Medium-and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleukodystrophy;Rocchiccioli;Pediatr Res,1986
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