Jou, Shuo-Bin <br/><br/>
Novel CLCN1 mutations in Taiwanese patients with myotonia congenita.  [electronic resource] 

 -  Journal of neurology  Jun 2004 
 - 666-70 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-5354 
<br/><br/><label>Standard No.: </label>10.1007/s00415-004-0383-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aspartic Acid--genetics<br/>Child<br/>Chloride Channels--genetics<br/>DNA Mutational Analysis--methods<br/>Female<br/>Glycine--genetics<br/>Humans<br/>Isoleucine--genetics<br/>Male<br/>Mutation, Missense<br/>Myotonia Congenita--genetics<br/>Phenylalanine--genetics<br/>Polymorphism, Genetic<br/>Proline--genetics<br/>Serine--genetics<br/>Taiwan--epidemiology<br/>Threonine--genetics