✦ LIBER ✦

Loss-of-function mutations of the K+ channel gene KCNJ2 constitute a rare cause of long QT syndrome

✍ Scribed by Heidi Fodstad; Heikki Swan; Muriel Auberson; Ivan Gautschi; Johannes Loffing; Laurent Schild; Kimmo Kontula

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Long QT syndrome with cardiac arrest and

✍ De Ferrari, Gaetano M.; Crotti, Lia; Lundquist, Andrew L.; Pedrazzini, Matteo; I 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 77 KB

Congenital long QT syndrome caused by th

✍ Wei Li; Qiu-fen Wang; Rong Du; Qiu-Mei Xu; Qin-Mei Ke; Bin Wang; Xue-Lin Chen; L 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 657 KB

G022 Loss-of-function mutation of the ca

✍ M. Amarouch; J. Barc; D. Béziau; F. Kyndt; H. Le Marec; D. Babuty; V. Probst; J. 📂 Article 📅 2009 🏛 Elsevier 🌐 English ⚖ 70 KB

Heterozygous mutation in the pore of pot

✍ Neyroud, Nathalie; Denjoy, Isabelle; Donger, Claire; Gary, Françoise; Villain, E 📂 Article 📅 1998 🏛 Nature Publishing Group 🌐 English ⚖ 243 KB

A loss of function mutation in the COL9A

✍ Stuart Baker; Carol Booth; Corrine Fillman; Michael Shapiro; Michael P. Blair; J 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 561 KB

A novel mutation in the transmembrane no

✍ Liu, Li; Hayashi, Kenshi; Kaneda, Tomoya; Ino, Hidekazu; Fujino, Noboru; Uchiyam 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 751 KB