Hereditary systemic amyloidosis associated with a new apolipoprotein AII stop codon mutation Stop78Arg

Hereditary systemic amyloidosis associated with a new apolipoprotein AII stop codon mutation Stop78Arg. Mutations in the gene for apolipoprotein AII (apoAII) have recently been found to cause hereditary renal amyloidosis. In each case amyloid deposition has been associated with a peptide extension a...

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Veröffentlicht in:Kidney international 2003-07, Vol.64 (1), p.11-16
Hauptverfasser: Yazaki, Masahide, Liepnieks, Juris J., Barats, Mark S., Cohen, Arthur H., Benson, Merrill D.
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Sprache:eng
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