Genetic peroxisomal disorders: Why, when, and how to test
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference14 articles.
1. Rat liver peroxisomes catalyze the beta oxidation of fatty acids.
2. Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome
3. BIOCHEMISTRY OF PEROXISOMES
4. A mouse model for X-linked adrenoleukodystrophy
5. Targeted Deletion of the PEX2 Peroxisome Assembly Gene in Mice Provides a Model for Zellweger Syndrome, a Human Neuronal Migration Disorder
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Metabolic neuropathies and myopathies;Handbook of Clinical Neurology;2013
2. Peroxisomal Disorders;Swaiman's Pediatric Neurology;2012
3. The Skin as a Clue for the Diagnosis of Inherited Metabolic Disorders;Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes;2008
4. Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders;The American Journal of Human Genetics;2002-06
5. Peroxisomes in Dermatology. Part II;Journal of Cutaneous Medicine and Surgery: Incorporating Medical and Surgical Dermatology;2001-08-01
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