Novel CLCN1 mutations in Taiwanese patients with myotonia congenita. [electronic resource]
Producer: 20040928Description: 666-70 p. digitalISSN:- 0340-5354
- Adolescent
- Adult
- Aspartic Acid -- genetics
- Child
- Chloride Channels -- genetics
- DNA Mutational Analysis -- methods
- Female
- Glycine -- genetics
- Humans
- Isoleucine -- genetics
- Male
- Mutation, Missense
- Myotonia Congenita -- genetics
- Phenylalanine -- genetics
- Polymorphism, Genetic
- Proline -- genetics
- Serine -- genetics
- Taiwan -- epidemiology
- Threonine -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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