Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

✍ Scribed by Browne, David L.; Gancher, Stephen T.; Nutt, John G.; Brunt, Ewout R. P.; Smith, Eric A.; Kramer, Patricia; Litt, Michael

• Book ID: 109918240
• Publisher: Nature Publishing Group
• Year: 1994
• Tongue: English
• Weight: 494 KB
• Volume: 8
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng1094-136