about
Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.Sarcomeric gene mutations in sudden infant death syndrome (SIDS).Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood.Prospective and Retrospective Diagnosis of Barth Syndrome Aided by Next-Generation Sequencing.Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disordersInvolvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS)Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Montserrat Santori
@ast
Montserrat Santori
@en
Montserrat Santori
@es
Montserrat Santori
@nl
Montserrat Santori
@sl
type
label
Montserrat Santori
@ast
Montserrat Santori
@en
Montserrat Santori
@es
Montserrat Santori
@nl
Montserrat Santori
@sl
prefLabel
Montserrat Santori
@ast
Montserrat Santori
@en
Montserrat Santori
@es
Montserrat Santori
@nl
Montserrat Santori
@sl
P106
P21
P31
P496
0000-0002-7721-1194