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3.6.4.6
medicine
diagnosis, HsPex6p mutations are one of the causes of Zellweger syndrome
210580
3.6.4.6
medicine
dysfunction of p97 has serious pathological consequences and has been implicated in a variety of cancers and neurodegenerative deseases
688690
3.6.4.6
medicine
HsPEX1 is the causative gene for peroxisome-deficiency autosomal recessive disorders like cerebro-hepato-renal Zellweger syndrome, neonatal adrenoleukodystrophy and infantile refsum disease
210581
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210583
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