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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From the \*Divisione di Cardiologia, Ospedale "G. da Procida," Salerno, Italy and tDivisione di Ostetricia e Ginecologia, Ospedale di Terlizzi,
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