Functional characterization of a novel frameshift mutation in the C-terminus of the Nav1.5 channel underlying a Brugada syndrome with variable expression in a Spanish family.
about
Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.Calcium in Brugada Syndrome: Questions for Future ResearchComplex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutationsBrugada syndrome trafficking-defective Nav1.5 channels can trap cardiac Kir2.1/2.2 channels
P2860
Functional characterization of a novel frameshift mutation in the C-terminus of the Nav1.5 channel underlying a Brugada syndrome with variable expression in a Spanish family.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Functional characterization of ...... xpression in a Spanish family.
@ast
Functional characterization of ...... xpression in a Spanish family.
@en
type
label
Functional characterization of ...... xpression in a Spanish family.
@ast
Functional characterization of ...... xpression in a Spanish family.
@en
prefLabel
Functional characterization of ...... xpression in a Spanish family.
@ast
Functional characterization of ...... xpression in a Spanish family.
@en
P2093
P2860
P50
P1433
P1476
Functional characterization of ...... xpression in a Spanish family.
@en
P2093
Adriana Barana
Irene Amorós
Juan Jiménez-Jáimez
Lucía Núñez
Luis Tercedor-Sánchez
Marcos Matamoros
Marta González de la Fuente
Marta Pérez-Hernández
Mercedes Núñez
Miguel Alvarez-López
P2860
P304
P356
10.1371/JOURNAL.PONE.0081493
P407
P577
2013-11-25T00:00:00Z