Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants
about
Analbuminemia: three cases resulting from different point mutations in the albumin geneA nucleotide insertion and frameshift cause analbuminemia in an Italian familyGenetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.cDNA and protein sequence of polymorphic macaque albumins that differ in bilirubin binding.Determination of true ratios of different N-glycan structures in electrospray ionization mass spectrometry.Detection of hereditary bisalbuminemia in a Greek family by capillary zone electrophoresis.
P2860
Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on September 1992
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Alloalbuminemia in Sweden: str ...... ution of nine albumin variants
@en
Alloalbuminemia in Sweden: str ...... tion of nine albumin variants.
@nl
type
label
Alloalbuminemia in Sweden: str ...... ution of nine albumin variants
@en
Alloalbuminemia in Sweden: str ...... tion of nine albumin variants.
@nl
prefLabel
Alloalbuminemia in Sweden: str ...... ution of nine albumin variants
@en
Alloalbuminemia in Sweden: str ...... tion of nine albumin variants.
@nl
P2093
P2860
P356
P1476
Alloalbuminemia in Sweden: str ...... ution of nine albumin variants
@en
P2093
P2860
P304
P356
10.1073/PNAS.89.17.8225
P407
P577
1992-09-01T00:00:00Z