Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8669116 | Journal of Electrocardiology | 2017 | 22 Pages |
Abstract
Identification of the novel mutation not only supports the genetic testing as a definitive diagnostic tool for detection of at risk family members, but also emphasizes its screening in Iranian LQTS patients as this mutation is very likely a founder mutation in Iran.
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Authors
Zahra Zafari, Mohammad Dalili, Sirus Zeinali, Siamak Saber, Amir Farjam Fazeli Far, Mohammad Taghi Akbari,