Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen–Tawil syndrome

By Ördög Balázs   Hategan Lidia   Kovács Mária   Seprényi György   Kohajda Zsófia   Nagy István   Hegedűs Zoltán   Környei László   Jost Norbert   Katona Márta   Szekeres Miklós   Forster Tamás   Papp Julius Gy.   Varró András   Sepp Róbert  

Canadian Journal of Physiology and Pharmacology, Vol. 93, Iss. 7, 2015-01 ,pp. : 569-575

NRC Research Press

Access to resources Recommend Favorite

Effect of Flecainide on T-Wave Alternans in Andersen–Tawil Syndrome

By Hayashi Hideki   Kawaguchi Tamiro   Horie Minoru  

Annals of Noninvasive Electrocardiology, Vol. 19, Iss. 4, 2014-07 ,pp. : 383-386

Blackwell Publishing

Access to resources Recommend Favorite

Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A

By Calloe Kirstine   Schmitt Nicole   Grubb Soren   Pfeiffer Ryan   David Jens-Peter   Kanter Ronald   Cordeiro Jonathan M.   Antzelevitch Charles  

Canadian Journal of Physiology and Pharmacology, Vol. 89, Iss. 10, 2011-10 ,pp. : 723-736

NRC Research Press

Access to resources Recommend Favorite

Smith‐Lemli‐Opitz syndrome: New mutation with a mild phenotype

By  

American Journal of Medical Genetics, Vol. 108, Iss. 1, 2002-02 ,pp. : 64-68

John Wiley & Sons Inc

Access to resources Recommend Favorite

Neuroleptic Malignant Syndrome Associated with Atypical Antipsychotic Drugs

By Trollor Julian N.   Chen Xiaohua   Sachdev Perminder S.  

CNS Drugs, Vol. 23, Iss. 6, 2009-05 ,pp. : 477-492

Adis International

Access to resources Recommend Favorite