Association between genetic variation of CACNA1H and childhood absence epilepsy. [electronic resource]
Producer: 20040105Description: 239-43 p. digitalISSN:- 0364-5134
- Age of Onset
- Amino Acid Substitution
- Calcium Channels, T-Type -- genetics
- Child
- Child, Preschool
- China
- DNA -- genetics
- Electroencephalography
- Epilepsy, Absence -- genetics
- Exons -- genetics
- Female
- Genetic Variation
- Humans
- Male
- Mutation, Missense -- genetics
- Reverse Transcriptase Polymerase Chain Reaction
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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