Forsyth, Rob J <br/><br/>
A novel GLRA1 mutation in a recessive hyperekplexia pedigree.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Aug 2007 
 - 1643-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0885-3185 
<br/><br/><label>Standard No.: </label>10.1002/mds.21574  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Cysteine--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Movement Disorders--genetics<br/>Mutation--genetics<br/>Pedigree<br/>Receptors, Glycine--genetics<br/>Reflex, Startle--genetics<br/>Tyrosine--genetics