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Results 1 - 3 of 3
EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.6.4.6medicine diagnosis, HsPex6p mutations are one of the causes of Zellweger syndrome 210580
Display the word mapDisplay the reaction diagram Show all sequences 3.6.4.6medicine dysfunction of p97 has serious pathological consequences and has been implicated in a variety of cancers and neurodegenerative deseases 688690
Display the word mapDisplay the reaction diagram Show all sequences 3.6.4.6medicine HsPEX1 is the causative gene for peroxisome-deficiency autosomal recessive disorders like cerebro-hepato-renal Zellweger syndrome, neonatal adrenoleukodystrophy and infantile refsum disease 210581, 210583
Results 1 - 3 of 3