Organ Transplantation in Hereditary Fibrinogen A α-Chain Amyloidosis: A Case Series of French Patients-Reference-Cited by-同舟云学术

Organ Transplantation in Hereditary Fibrinogen A α-Chain Amyloidosis: A Case Series of French Patients

Published:2020-09 Issue:3 Volume:76 Page:384-391
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Meyer Lara,Ulrich Marc,Ducloux Didier,Garrigue Valérie,Vigneau Cécile,Nochy Dominique,Bobrie Guillaume,Ferlicot Sophie,Colombat Magalie,Boffa Jean-Jacques,Clabault Karine,Mansour Jeannette,Mousson Christiane,Azar Raymond,Bacri Jean-Louis,Dürrbach Antoine,Duvic Christian,El Karoui Khalil,Hoffmann Maxime,Lionet Arnaud,Panescu Victor,Plaisier Emmanuelle,Ratsimbazafy Anderson,Guerrot Dominique,Vrigneaud Laurence,Valleix Sophie,François Hélène^ORCID

Publisher

Elsevier BV

Subject

Nephrology

Reference28 articles.

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

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

3. A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene;Benson;Genomics,2001

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

5. Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline;Mauri;Biochim Biophys Acta,1990

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