Frédéric, Mélissa <br/><br/>
First determination of the incidence of the unique TOR1A gene mutation, c.907delGAG, in a Mediterranean population.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Apr 2007 
 - 884-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0885-3185 
<br/><br/><label>Standard No.: </label>10.1002/mds.21391  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA--blood<br/>France<br/>Gene Amplification<br/>Humans<br/>Incidence<br/>Infant, Newborn<br/>Mediterranean Islands<br/>Molecular Chaperones--genetics<br/>Mutation<br/>Sequence Deletion