Mercier, Sandra <br/><br/>
Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.  [electronic resource] 

 -  European journal of human genetics : EJHG  Aug 2013 
 - 855-63 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2012.269  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aged<br/>Biopsy<br/>Blotting, Western<br/>Child<br/>Child, Preschool<br/>Cognition Disorders--genetics<br/>Dystrophin--genetics<br/>Female<br/>France--epidemiology<br/>Heterozygote<br/>Humans<br/>Immunohistochemistry<br/>Middle Aged<br/>Muscles--metabolism<br/>Muscular Dystrophy, Duchenne--epidemiology<br/>Mutation<br/>X Chromosome Inactivation<br/>Young Adult