about
Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) casesErratum to: Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) casesFunctional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death
P50
Q39192594-72FFBCE8-3AB9-488B-825B-0D2472FE0601Q49924734-AAA6B03B-BDC5-48E9-B6F7-627A50B984DBQ53582870-4E441E43-016E-46B6-9816-91B86B13C849Q55339082-183C991F-B708-4FC5-9CA7-26D5064AE612Q60998047-9941D143-310B-4AA0-9E35-CF493FE86867Q60998048-0624D811-2E72-470A-9C30-AAACF2B4784DQ92915179-48831959-BC9A-47D4-A8EA-25EFC6D65EEB
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Jacqueline Neubauer
@en
Jacqueline Neubauer
@nl
type
label
Jacqueline Neubauer
@en
Jacqueline Neubauer
@nl
prefLabel
Jacqueline Neubauer
@en
Jacqueline Neubauer
@nl
P31
P496
0000-0002-9472-7803