Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy
izdano v: | Molecular genetics & genomic medicine 7(2019)8, S. e841 |
---|---|
VerfasserIn: | Gaertner-Rommel, Anna (VerfasserIn), Tiesmeier, Jens (VerfasserIn), Jacob, Thomas (VerfasserIn) |
Format: | Aufsatz in Zeitschrift |
Jezik: | English |
Izdano: |
2019
|
Teme: | |
Online dostop: | https://doi.org/10.1002/mgg3.841 |
Sorodne knjige/članki: | In:
Molecular genetics & genomic medicine |
Podobne knjige/članki
-
Interrupted Chain of Transmission in a Pediatric COVID-19 Case
od: Grautoff, Steffen
Izdano: (2020) -
The emergency medical service has a crucial role to unravel the genetics of sudden cardiac arrest in young, out of hospital resuscitated patients: Interim data from the MAP-IT study
od: Tiesmeier, Jens, et al.
Izdano: (2021) -
Case report: Early detection of mesenteric ischemia by intravital microscopy in a patient with septic shock
od: Praxenthaler, Janina, et al.
Izdano: (2022) -
Wellens' syndrome can indicate high-grade LAD stenosis in case of left bundle branch block
od: Grautoff, Steffen
Izdano: (2017) -
Profound decrease of liver maximum function capacity test of isoflurane sedated patients : a report of three cases
od: Schwier, Elke, et al.
Izdano: (2021)