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Volumn 99, Issue 4, 2006, Pages 274-
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Hereditary renal amyloidosis associated with a novel mutation in the apolipoprotein AII gene [2]
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Author keywords
[No Author keywords available]
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Indexed keywords
AMYLOID;
APOLIPOPROTEIN A2;
ARGININE;
GLYCINE;
PREALBUMIN;
SERINE;
ADULT;
CASE REPORT;
DISEASE COURSE;
DNA DETERMINATION;
FOLLOW UP;
GENE MUTATION;
GENETIC CODE;
GENETIC DISORDER;
GENETIC RISK;
HUMAN;
HUMAN TISSUE;
IMMUNOHISTOCHEMISTRY;
KIDNEY AMYLOIDOSIS;
KIDNEY BIOPSY;
KIDNEY FAILURE;
KIDNEY TRANSPLANTATION;
LETTER;
LIVER TRANSPLANTATION;
MALE;
MUTATIONAL ANALYSIS;
NEPHROTIC SYNDROME;
NUCLEIC ACID BASE SUBSTITUTION;
PRIORITY JOURNAL;
PROTEIN SYNTHESIS;
PROTEIN VARIANT;
STOP CODON;
TREATMENT INDICATION;
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EID: 33645554421
PISSN: 14602725
EISSN: 14602393
Source Type: Journal
DOI: 10.1093/qjmed/hcl032 Document Type: Letter |
Times cited : (6)
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References (5)
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