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De novo mutation responsible for atrial fibrillation in utero

✍ Scribed by Hong, Kui; Piper, David R.; Diaz-Valdecantos, Aurora; Brugada, Josep; Burashnikov, Elena; Santos-De-soto, José; Grueso-Montero, Josefina; Brugada, Pedro; Sanguinetti, Michael C.; Brugada, Ramón


Book ID
122459556
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
59 KB
Volume
2
Category
Article
ISSN
1547-5271

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✍ Yue, Qing; Jen, Joanna C.; Thwe, May Myo; Nelson, Stanley F.; Baloh, Robert W. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 13 KB 👁 2 views

With the recent report of mutations in the calcium channel gene CACNA1A in two families with episodic ataxia type 2, we investigated a patient with nonfamilial episodic vertigo and ataxia responsive to acetazolamide for similar mutations. Singlestrand conformation polymorphism (SSCP) analysis of exo