3-Hydroxydicarboxylic aciduria: A distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01811422
Reference4 articles.
1. Greter, J., Lindstedt, S., Seeman, H. and Steen, G. 3-Hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis.Clin. Chem. 26 (1980) 261–265
2. Mortensen, P. B. Dicarboxylic acids and the lipid metabolism.Dan. Med. Bull. 31 (1980) 121–145
3. Riudor, E., Ribes, A., Boronat, M., Sabado, C., Dominguez, C. and Ballabriga, A. A new case of C6–C14 dicarboxylic aciduria with favourable evolution.J. Inher. Metab. Dis. 9 Suppl. 2 (1986) 297–299
4. Rocchiccioli, F., Aubourg, P. and Bougnères, P. F. Medium-and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleucodystrophy.Pediatr. Res. 20 (1986) 62–66
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