Normal and Aberrant Biological Self-Assembly: Insights from Studies of Human Lysozyme and Its Amyloidogenic Variants
Author:
Affiliation:
1. Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ar050070g
Reference37 articles.
1. Human lysozyme gene mutations cause hereditary systemic amyloidosis
2. Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family
3. A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis
4. A novel variant of human lysozyme (T70N) is common in the normal population
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