Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy (vol 47, pg 73, 2015)

被引:4
作者
Simons, Cas
Rash, Lachlan D.
Crawford, Joanna
Ma, Linlin
Cristofori-Armstrong, Ben
Miller, David
Ru, Kelin
Baillie, Gregory J.
Alanay, Yasemin
Jacquinet, Adeline
Debray, Franois-Guillaume
Verloes, Alain
Shen, Joseph
Yesil, Goezde
Guler, Serhat
Yuksel, Adnan
Cleary, John G.
Grimmond, Sean M.
McGaughran, Julie
King, Glenn F.
Gabbett, Michael T.
Taft, Ryan J.
机构
关键词
D O I
10.1038/ng0315-304b
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nat. Genet. 47, 73–77 (2015); published online 24 November 2014; corrected after print 6 February 2015 In the version of this article initially published, in Figure 2a, the order of the protein alterations for variants c.1465C>T and c.1480A>G was inverted. The correct protein alterations for these two variants are p.
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页码:304 / 304
页数:1
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  • [2] Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy
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