Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations. [electronic resource]
Producer: 20061108Description: 1159-64 p. digitalISSN:- 1526-632X
- Base Sequence
- Child
- DNA Mutational Analysis
- Europe -- epidemiology
- Genetic Predisposition to Disease -- epidemiology
- Humans
- Molecular Sequence Data
- Multigene Family -- genetics
- Muscle Proteins -- genetics
- Mutation
- Myasthenic Syndromes, Congenital -- epidemiology
- Polymorphism, Single Nucleotide -- genetics
- Receptors, Nicotinic -- genetics
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Publication Type: Controlled Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
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