Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia
about
New insights on hereditary erythrocyte membrane defectsDisorders of erythrocyte hydration.Hereditary stomatocytosis: An underdiagnosed condition.PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis.The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.Erythrocytes lacking the Langereis blood group protein ABCB6 are resistant to the malaria parasite
P2860
Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 05 May 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Functional characterization of ...... in familial pseudohyperkalemia
@en
Functional characterization of ...... n familial pseudohyperkalemia.
@nl
type
label
Functional characterization of ...... in familial pseudohyperkalemia
@en
Functional characterization of ...... n familial pseudohyperkalemia.
@nl
prefLabel
Functional characterization of ...... in familial pseudohyperkalemia
@en
Functional characterization of ...... n familial pseudohyperkalemia.
@nl
P2093
P2860
P50
P1433
P1476
Functional characterization of ...... in familial pseudohyperkalemia
@en
P2093
Achille Iolascon
Alok K Sharma
Antonella Gambale
Carlo Brugnara
Catia Lo Pardo
Gianluca De Rosa
Lucia De Franceschi
Seth L Alper
Soha Zouwail
P2860
P304
P356
10.3324/HAEMATOL.2016.142372
P577
2016-05-05T00:00:00Z