A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. [electronic resource]
Producer: 20090728Description: 778-82 p. digitalISSN:- 1531-8257
- Adult
- Animals
- CHO Cells
- Cerebellar Diseases -- genetics
- Child, Preschool
- Cricetinae
- Cricetulus
- DNA Mutational Analysis -- methods
- Female
- Genetic Predisposition to Disease
- Humans
- Kv1.1 Potassium Channel -- genetics
- Leucine -- genetics
- Magnetic Resonance Imaging -- methods
- Male
- Membrane Potentials -- genetics
- Mutation -- genetics
- Transfection -- methods
- Valine -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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