Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.
about
Forensic genetics and genomics: Much more than just a human affair.Application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death.Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?Sudden infant death syndrome and inherited cardiac conditions.Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases.Molecular genetic diagnostics for ventricular arrhythmias and sudden cardiac death syndromes.Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea
P2860
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P2860
Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.
description
2017 nî lūn-bûn
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name
Post-mortem whole-exome analys ...... nd metabolic genetic diseases.
@en
Post-mortem whole-exome analys ...... nd metabolic genetic diseases.
@nl
type
label
Post-mortem whole-exome analys ...... nd metabolic genetic diseases.
@en
Post-mortem whole-exome analys ...... nd metabolic genetic diseases.
@nl
prefLabel
Post-mortem whole-exome analys ...... nd metabolic genetic diseases.
@en
Post-mortem whole-exome analys ...... nd metabolic genetic diseases.
@nl
P2093
P2860
P50
P356
P1476
Post-mortem whole-exome analys ...... and metabolic genetic diseases
@en
P2093
Christine Bartsch
Giancarlo Russo
Maria Rita Lecca
Wolfgang Berger
P2860
P2888
P304
P356
10.1038/EJHG.2016.199
P577
2017-01-11T00:00:00Z