Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome. [electronic resource]
Producer: 20130409Description: e41802 p. digitalISSN:- 1932-6203
- Adolescent
- Amino Acid Sequence
- Animals
- Asian People -- genetics
- Base Sequence
- Cadherins -- chemistry
- Child
- Child, Preschool
- DNA Mutational Analysis
- Epilepsies, Myoclonic -- complications
- Female
- Humans
- Infant
- Intellectual Disability -- complications
- Male
- Mutation
- Mutation, Missense -- genetics
- NAV1.1 Voltage-Gated Sodium Channel -- chemistry
- Nuclear Proteins -- chemistry
- Phenotype
- Polymorphism, Genetic -- genetics
- Protocadherins
- RNA Splice Sites -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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