The Neuronal Migration Defect in Mice with Zellweger Syndrome (Pex5Knockout) is not Caused by the Inactivity of Peroxisomal β-Oxidation

Author:

Baes M.,Gressens P.,Huyghe S.,De Nys K.,Qi C.,Jia Y.,Mannaerts G. P.,Evrard P.,Van Veldhoven P. P.,Declercq P. E.,Reddy J. K.

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Reference30 articles.

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3. Structural and Chemical Alterations in the Cerebral Maldevelopment of Fetal Cerebro-Hepato-Renal (Zellweger) Syndrome

4. Polyunsaturated fatty acids in the developing human brain, erythrocytes and plasma in peroxisomal disease: Therapeutic implications;Martinez;J Inherit Metab Dis,1995

5. Wanders RJA Barth PG Heymans HHA . Single peroxisomal enzyme deficiencies. In: Scriver Beaudet Valle Sly , eds. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill, 2001:3219–56

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