Pradhan_2021_BMJ.Case.Rep_14_

Reference

Title : Hereditary pseudocholinesterase deficiency discovery after electroconvulsive therapy - Pradhan_2021_BMJ.Case.Rep_14_
Author(s) : Pradhan BK , van Helmond N , Mitrev LV , Andonakakis AA
Ref : BMJ Case Rep , 14 : , 2021
Abstract : Pradhan_2021_BMJ.Case.Rep_14_
ESTHER : Pradhan_2021_BMJ.Case.Rep_14_
PubMedSearch : Pradhan_2021_BMJ.Case.Rep_14_
PubMedID: 33462045

Related information

Citations formats

Pradhan BK, van Helmond N, Mitrev LV, Andonakakis AA (2021)
Hereditary pseudocholinesterase deficiency discovery after electroconvulsive therapy
BMJ Case Rep 14 :

Pradhan BK, van Helmond N, Mitrev LV, Andonakakis AA (2021)
BMJ Case Rep 14 :