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A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis

Masahide Yazaki, Sandra A. Farrell, Merrill D. Benson

Kidney International · 2003 · 118 citations · 20 references

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References

20

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

David R. Booth, Margaret Sunde, Vittorio Bellotti et al. · Nature · 1997 · 1K citations

, , +14

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 660 citations

, , +12

<i>Trans</i> -Suppression of Misfolding in an Amyloid Disease

Per Hammarström, Frank Schneider, Jeffery W. Kelly · Science · 2001 · 291 citations

, , +17

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

William C. Nichols, Francis E. Dwulet, Juris J. Liepnieks et al. · Biochemical and Biophysical Research Communications · 1988 · 233 citations

, , +15

Hereditary renal amyloidosis associated with a mutant fibrinogen α–chain

Merrill D. Benson, Juris J. Liepnieks, Tomoyuki Uemichi et al. · Nature Genetics · 1993 · 218 citations

, , +14