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PM025 A Severe Type of Long QT Syndrome and Cardiovascular Anomaly in a Homozygous Carrier of a Novel KCNH2 Mutation and Findings in Family Screening

✍ Scribed by Al-Senaidi, Khalfan S.; Wang, Guoliang; Zhang, Li; Beer, Dominik A.; Al-Farqani, Abdullah M.; Al-Maskaryi, Salim N.; Penny, Daniel J.; Kowey, Peter R.; Fan, Yuxin

Book ID: 122194525
Publisher: Elsevier
Year: 2014
Tongue: English
Weight: 305 KB
Volume: 9
Category: Article
ISSN: 2211-8160
DOI: 10.1016/j.gheart.2014.03.1444

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