Cho, H-J <br/><br/>
Mitochondrial GTPase mitofusin 2 mutations in Korean patients with Charcot-Marie-Tooth neuropathy type 2.  [electronic resource] 

 -  Clinical genetics  Mar 2007 
 - 267-72 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2007.00763.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Asian People<br/>Base Sequence<br/>Charcot-Marie-Tooth Disease--diagnosis<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Infant<br/>Male<br/>Membrane Proteins--genetics<br/>Mitochondrial Proteins--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree