A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis-Reference-Cited by-同舟云学术

A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis

Published:2003-05 Issue:5 Volume:63 Page:1652-1657
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

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

Publisher

Elsevier BV

Subject

Nephrology

Reference22 articles.

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3. Variant apoprotein AI as a major constituent of a human hereditary amyloid;Nichols;Biochem Biophys Res Commun,1988

4. Hereditary renal amyloidosis associated with a mutant fibrinogen α-chain;Benson;Nat Genet,1993

5. Human lysozyme gene mutations cause hereditary systemic amyloidosis;Pepys;Nature,1993

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