A novel mutation in the cardiac ryanodine receptor gene (RyR2) in a patient with an unequivocal LQTS

International Journal of Cardiology

Volumn 146, Issue 2, 2011, Pages 249-250

  Kauferstein, Silke ^a   Kiehne, Nadine ^a   Erkapic, Damir ^b   Schmidt, Jörn ^b   Hamm, Christian W ^b   Bratzke, Hansjürgen ^a   Pitschner, Heinz Friedrich ^b   Kuniss, Malte ^b   Neumann, Thomas ^b  

^a GOETHE UNIVERSITY   (Germany)

^b KERCKHOFF HEART CENTER   (Germany)

Author keywords

Channelopathies; Genetic testing; Long QT syndrome; Ryanodine receptor; Sudden cardiac death

Indexed keywords

ATENOLOL; RYANODINE RECEPTOR 2;

ADULT; CASE REPORT; DEFIBRILLATOR; ELECTROCARDIOGRAM; FEMALE; GENETIC SCREENING; HUMAN; LETTER; LONG QT SYNDROME; MISSENSE MUTATION; PRIORITY JOURNAL; SCORING SYSTEM; SYNCOPE;

EID: 78651434300     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2010.10.062     Document Type: Article

References (6)

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