Disorders of peroxisome biogenesis: Complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)

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Veröffentlicht in:	Journal of inherited metabolic disease 1999-05, Vol.22 (3), p.314-318
Hauptverfasser:	Wanders, R. J. A., Mooijer, P. A. W., Dekker, C., Suzuki, Y., Shimozawa, N.
Format:	Artikel
Sprache:	eng
Schlagworte:	ATPases Associated with Diverse Cellular Activities Biological and medical sciences Catalase - analysis Errors of metabolism Genetic Complementation Test Genetic Heterogeneity Humans Lipids (lysosomal enzyme disorders, storage diseases) Medical sciences Membrane Proteins - genetics Metabolic diseases Microbodies Microscopy, Fluorescence Peroxisomal Disorders - genetics Zellweger Syndrome - genetics
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