Sarret, Catherine <br/><br/>
Sjögren-Larsson syndrome: novel mutations in the ALDH3A2 gene in a French cohort.  [electronic resource] 

 -  Journal of the neurological sciences  Jan 2012 
 - 123-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1878-5883 
<br/><br/><label>Standard No.: </label>10.1016/j.jns.2011.08.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Aldehyde Oxidoreductases--genetics<br/>Child<br/>Cohort Studies<br/>Female<br/>France<br/>Humans<br/>Infant<br/>Male<br/>Point Mutation--genetics<br/>Radiography<br/>Sjogren-Larsson Syndrome--diagnostic imaging