TY - JOUR
TI - Hereditary systemic amyloidosis caused by K19T apolipoprotein C-II variant
AU - Liapis, K.
AU - Panagopoulou, P.
AU - Charitaki, E.
AU - Rowczenio, D.
AU - Gilbertson, J.
AU - Papathoma, A.
AU - Kostopoulou, M.
AU - Dimopoulos, M.A.
AU - Gillmore, J.D.
AU - Kastritis, E.
JO - Amyloid: The Journal of Protein Folding Disorders
PY - 2019
VL - 26
TODO - 1
SP - 52-53
PB - Taylor and Francis Ltd.
SN - 1350-6129, 1744-2818
TODO - 10.1080/13506129.2018.1562442
TODO - amyloid;  apolipoprotein C2;  creatinine;  genomic DNA;  lysine;  threonine;  apolipoprotein C2, abdominal fat;  aged;  case report;  chronic kidney failure;  clinical article;  creatinine blood level;  exon;  familial amyloidosis;  genetic variability;  human;  human tissue;  hypertension;  immunohistochemistry;  Letter;  male;  medical history;  priority journal;  protein electrophoresis;  very elderly;  familial amyloidosis;  genetics;  metabolism;  mutation, Aged, 80 and over;  Amyloidosis, Familial;  Apolipoprotein C-II;  Humans;  Male;  Mutation
TODO - null
ER -