Lesca, G <br/><br/>
[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias].  [electronic resource] 

 -  Revue neurologique  Sep 2003 
 - 775-80 p.  digital 
<br/><br/> Publication Type: Case Reports; English Abstract; Journal Article 
<br/><br/><label>ISSN: </label>0035-3787 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Chromosomes, Human, X--genetics<br/>Codon, Terminator--genetics<br/>Dystrophin--genetics<br/>Exons<br/>Family<br/>Female<br/>Gene Silencing<br/>Heterozygote<br/>Humans<br/>Immunohistochemistry<br/>Male<br/>Middle Aged<br/>Muscle Weakness--etiology<br/>Muscle, Skeletal--pathology<br/>Muscular Dystrophies--genetics<br/>Muscular Dystrophy, Duchenne--genetics<br/>Pedigree