Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand

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Bibliographic Details
Published in:	Circulation. Genomic and precision medicine Vol. 14; no. 3; p. e003229
Main Authors:	Chimparlee, Nitinan, Prechawat, Somchai, Khongphatthanayothin, Apichai, Mauleekoonphairoj, John, Lekchuensakul, Sarin, Wongcharoen, Wanwarang, Makarawate, Pattarapong, Sahasatas, Dujdao, Krittayaphong, Rungroj, Amnueypol, Montawatt, Anannab, Alisara, Ngarmukos, Tachapong, Vardhanabhuti, Saran, Sutjaporn, Boosamas, Wandee, Pharawee, Veerakul, Gumpanart, Bezzina, Connie R., Poovorawan, Yong, Nademanee, Koonlawee
Format:	Journal Article
Language:	English
Published:	United States Lippincott Williams & Wilkins 01-06-2021
Subjects:	Adult Aged Amino Acid Substitution Brugada Syndrome - genetics Female Genetic Testing Humans Male Middle Aged Mutation, Missense NAV1.5 Voltage-Gated Sodium Channel - genetics Thailand Thailand phenotype ventricular fibrillation Brugada syndrome sodium channels Thailand gene frequency
Online Access:	Get full text
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Bibliography:	SourceType-Other Sources-1 content type line 63 ObjectType-Feature-2 ObjectType-Correspondence-1 ObjectType-Article-3
ISSN:	2574-8300 2574-8300
DOI:	10.1161/CIRCGEN.120.003229