The role of chaperone-assisted folding and quality control in inborn errors of metabolism: Protein folding disorders
Author:
Affiliation:
1. ; Research Unit for Molecular Medicine, Aarhus University Hospital and Faculty of Health Sciences; Aarhus University; Aarhus Denmark
2. ; Institute of Human Genetics; Aarhus University; Aarhus Denmark
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1010319001722/fullpdf
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4. Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed humanmedium-chain acyl-CoA dehydrogenase (MCAD) carrying the preva-lent disease-causing K304E mutation;Bross;Biochim Biophys Acta,1993
5. Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-defficient patients on folding, oligomer assembly, and stability of MCAD enzyme;Bross;J Biol Chem,1995
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