Peroxisomal Disorders: Genotype, Phenotype, Major Neuropathologic Lesions, and Pathogenesis
Author:
Publisher
Wiley
Subject
Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.1998.tb00139.x/fullpdf
Reference135 articles.
1. Rhizomelic chondrodysplasia punctata: report of a case with review of the literature and correlation with other peroxisomal disorders;Agamanolis;Ped Pathol Lab Med,1995
2. A mouse model for Zellweger syndrome;Baes;Nature Genet,1977
3. X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes;Berger;Biochem Biophys Res Commun,1994
4. Fatty acid composition of human proteolipid protein in peroxisomal disorders;Bizzozero;J Neurochem,1991
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