SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells

✍ Scribed by Ghayath Baroudi; Eric Carbonneau; Valérie Pouliot; Mohamed Chahine

• Book ID: 117101424
• Publisher: Elsevier Science
• Year: 2000
• Tongue: English
• Weight: 143 KB
• Volume: 467
• Category: Article
• ISSN: 0014-5793
• DOI: 10.1016/s0014-5793(00)01099-1