Molecular and clinical findings and diagnostic flowchart of peroxisomal diseases
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference21 articles.
1. Molecular and clinical aspects of peroxisomal diseases;Shimozawa;J Inher Metab Dis,2007
2. Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene;Shimozawa;Hum Mutat,2004
3. Peroxisome biogenesis disorders;Steinberg;Biochim Biophys Acta,2006
4. Genetic basis of peroxisome assembly mutants of humans, CHO cells and yeast: identification of a new complementation group of peroxisome biogenesis disorders, absent from peroxisomal membrane ghosts;Shimozawa;Am J Hum Genet,1998
5. A neurophysiological study of children with the cerebro-hepato-renal syndrome of Zellweger;Govaerts;Neuropediatrics,1985
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