Single Nucleotide Deletion Mutation of KCNH2 Gene is Responsible for LQT Syndrome in a 3-Generation Korean Family
2013 ◽
Vol 28
(9)
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pp. 1388
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Keyword(s):
1998 ◽
Vol 841
(1 MYASTHENIA GR)
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pp. 195-198
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Keyword(s):
2010 ◽
Vol 86
(4)
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pp. 596-603
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Keyword(s):
2003 ◽
Vol 525
(1-2)
◽
pp. 61-65
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2013 ◽
Vol 59
(9)
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pp. 967-973
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