Τίτλος:
Hereditary systemic amyloidosis caused by K19T apolipoprotein C-II variant
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Δεν υπάρχει περίληψη
Συγγραφείς:
Liapis, K.
Panagopoulou, P.
Charitaki, E.
Rowczenio, D.
Gilbertson, J.
Papathoma, A.
Kostopoulou, M.
Dimopoulos, M.A.
Gillmore, J.D.
Kastritis, E.
Περιοδικό:
Amyloid: The Journal of Protein Folding Disorders
Εκδότης:
Taylor and Francis Ltd.
Λέξεις-κλειδιά:
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
DOI:
10.1080/13506129.2018.1562442
