GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.
about
MUSCLEMOTION: A Versatile Open Software Tool to Quantify Cardiomyocyte and Cardiac Muscle Contraction In Vitro and In Vivo.A Genome-Wide Association Study and Complex Network Identify Four Core Hub Genes in Bipolar Disorder.On the Evolution of the Cardiac Pacemaker.Genome-Wide Identification and Characterization of WD40 Protein Genes in the Silkworm, Bombyx mori.Increased store-operated Ca2+ entry mediated by GNB5 and STIM1.
P2860
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 10 August 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
GNB5 Mutations Cause an Autoso ...... rdia and Cognitive Disability.
@en
GNB5 Mutations Cause an Autoso ...... rdia and Cognitive Disability.
@nl
type
label
GNB5 Mutations Cause an Autoso ...... rdia and Cognitive Disability.
@en
GNB5 Mutations Cause an Autoso ...... rdia and Cognitive Disability.
@nl
prefLabel
GNB5 Mutations Cause an Autoso ...... rdia and Cognitive Disability.
@en
GNB5 Mutations Cause an Autoso ...... rdia and Cognitive Disability.
@nl
P2093
P2860
P50
P1476
GNB5 Mutations Cause an Autoso ...... ardia and Cognitive Disability
@en
P2093
Alexandre Reymond
Barbara Mandriani
Carolina Fischinger Moura de Souza
Charlotte D Koopman
Connie R Bezzina
Eline A Nannenberg
Federico Tessadori
Fernando Kok
Giuseppe Merla
Ilham Ratbi
P2860
P304
P356
10.1016/J.AJHG.2016.06.025
P407
P50
P577
2016-08-11T00:00:00Z