Single nucleotide deletion mutation of KCNH2 gene is responsible for LQT syndrome in a 3-generation Korean family.

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Published in J Korean Med Sci on August 28, 2013

Authors

Jong Keun Park1, Yong-Seog Oh, Jee-hyun Choi, Sungjoo Kim Yoon

Author Affiliations

1: Department of Biomedical Sciences, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, Korea.

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