Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a french family

Kidney International

Volumn 61, Issue 3, 2002, Pages 907-912

  Valleix, Sophie ^a,b,c,d,e,f   Drunat, Séverine ^a,b,c,d,e,f   Philit, Jean Baptiste ^a,b,c,d,e,f   Adoue, Daniel ^a,b,c,d,e,f   Piette, Jean Charles ^a,b,c,d,e,f   Droz, Dominique ^a,b,c,d,e,f   Mac Gregor, Brigitte ^a,b,c,d,e,f   Canet, Denis ^a,b,c,d,e,f   Delpech, Marc ^a,b,c,d,e,f   Grateau, Gilles ^a,b,c,d,e,f  

^a Assistance Publique Hôpitaux de Paris ^*  (France)

^b HOSPICES CIVILS DE LYON   (France)

^c Toulouse University   (France)

^d SAINT LOUIS HOSPITAL   (France)

^e UNIVERSITY OF OXFORD   (United Kingdom)

^f HÔTEL DIEU   (France)

Author keywords

Amyloid; Gene mutation; Kidney; Lysozyme; Sicca syndrome

Indexed keywords

AMYLOID PROTEIN; APOLIPOPROTEIN A1; APOLIPOPROTEIN A2; CYSTATIN C; FIBRINOGEN; GELSOLIN; LYSOZYME; PEROXIDASE; PREALBUMIN;

AGED; AMINO ACID SUBSTITUTION; CASE REPORT; CONFERENCE PAPER; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; HUMAN; IMMUNOHISTOCHEMISTRY; INTESTINE; INTRON; KIDNEY; KIDNEY AMYLOIDOSIS; KIDNEY DISEASE; KIDNEY FAILURE; MALE; MUTATION; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PROCESSING; SALIVARY GLAND; SEQUENCE ANALYSIS; SJOEGREN SYNDROME;

EID: 0036189848     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2002.00205.x     Document Type: Article

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