Found: 6
Select item for more details and to access through your institution.
Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 23, p. 3565, doi. 10.1093/hmg/ddi384
- By:
- Publication type:
- Article
β-Ureidopropionase deficiency: A novel inborn error of metabolism discovered using NMR spectroscopy on urine.
- Published in:
- Magnetic Resonance in Medicine, 2001, v. 46, n. 5, p. 1014, doi. 10.1002/mrm.1289
- By:
- Publication type:
- Article
Human α-N-acetylgalactosaminidase (α-NAGA) deficiency: no association with neuroaxonal dystrophy?
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 91, doi. 10.1038/sj.ejhg.5200598
- By:
- Publication type:
- Article
Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 188, doi. 10.1038/72861
- By:
- Publication type:
- Article
Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects.
- Published in:
- British Journal of Clinical Pharmacology, 1998, v. 46, n. 2, p. 151, doi. 10.1046/j.1365-2125.1998.00751.x
- By:
- Publication type:
- Article
Known heat-shock proteins are not responsible for stress-induced rapid degradation of ribosomal protein mRNAs in yeast.
- Published in:
- Yeast, 1993, v. 9, n. 6, p. 583, doi. 10.1002/yea.320090604
- By:
- Publication type:
- Article