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Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders
Online Contents | 2002| -
Human Genome and Diseases: Review Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders
British Library Online Contents | 2002| -
Characterisation of the human 22 KD peroxisomal membrane protein gene
British Library Online Contents | 1998| -
Two different targeting signals direct human peroxisomal membrane protein 22 to peroxisomes
British Library Online Contents | 2002| -
The peroxisomal membrane targeting elements of human peroxin 2 (PEX2)
British Library Online Contents | 2003| -
Mutations in PEX1 in peroxisome biogenesis dosorders: G843D and a mild clinical phenotype
British Library Online Contents | 1999| -
Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70
British Library Online Contents | 1998| -
PEX1 Mutations in Complementation Group 1 of Zellweger Spectrum Patients Correlate with Severity of Disease
British Library Online Contents | 2002| -
Characterisation of the human 22 KD peroxisomal membrane protein gene
British Library Conference Proceedings | 1998| -
Mutations in human PEX1 in peroxisome biogenesis disorders
British Library Conference Proceedings | 1998| -
Peroxisome mosaicism in two PBD patients with mild clinical course and identical PEX1 mutations
British Library Conference Proceedings | 2000| -
The peroxisomal membrane targeting elements of human peroxin 2 (PEX2)
Online Contents | 2003|Contributors: Brosius, U. -
Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70
Online Contents | 1998|Contributors: Brosius, U.
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