Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy
Τόπος έκδοσης: | Molecular genetics & genomic medicine 7(2019)8, S. e841 |
---|---|
Κύριοι συγγραφείς: | Gaertner-Rommel, Anna (Συγγραφέας), Tiesmeier, Jens (Συγγραφέας), Jacob, Thomas (Συγγραφέας) |
Μορφή: | Άρθρο |
Γλώσσα: | English |
Έκδοση: |
2019
|
Θέματα: | |
Διαθέσιμο Online: | https://doi.org/10.1002/mgg3.841 |
Σχετικά τεκμήρια: | In:
Molecular genetics & genomic medicine |
Παρόμοια τεκμήρια
-
Interrupted Chain of Transmission in a Pediatric COVID-19 Case
ανά: Grautoff, Steffen
Έκδοση: (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
ανά: Tiesmeier, Jens, κ.ά.
Έκδοση: (2021) -
Case report: Early detection of mesenteric ischemia by intravital microscopy in a patient with septic shock
ανά: Praxenthaler, Janina, κ.ά.
Έκδοση: (2022) -
Wellens' syndrome can indicate high-grade LAD stenosis in case of left bundle branch block
ανά: Grautoff, Steffen
Έκδοση: (2017) -
Profound decrease of liver maximum function capacity test of isoflurane sedated patients : a report of three cases
ανά: Schwier, Elke, κ.ά.
Έκδοση: (2021)