Author | Title | Subject | Date | Publication Type | ||
---|---|---|---|---|---|---|
1 | Zhang, Jie. | Myotonia congenita-associated chloride channelopathies: mutations, function, and structure. | Physiology; Mutations | 1999-12 | dissertation | |
2 | Curran, Mark Edward | Molecular genetics of the long QT syndrome | Long QT Syndrome; Cardia Myocytes; Mutations | 1995-12 | dissertation |