Ifergane, G <br/><br/>
Co-morbidity of Emery-Dreifuss muscular dystrophy and a congenital myasthenic syndrome possibly affecting the phenotype in a large Bedouin kindred.  [electronic resource] 

 -  European journal of neurology  Mar 2007 
 - 305-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-1331 
<br/><br/><label>Standard No.: </label>10.1111/j.1468-1331.2006.01657.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Arabs--genetics<br/>Child<br/>Child, Preschool<br/>Comorbidity<br/>DNA Mutational Analysis<br/>Disease Progression<br/>Female<br/>Genetic Diseases, X-Linked--ethnology<br/>Genetic Linkage--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Genotype<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Muscle, Skeletal--innervation<br/>Muscular Dystrophy, Emery-Dreifuss--ethnology<br/>Myasthenic Syndromes, Congenital--ethnology<br/>Nuclear Proteins--genetics<br/>Pedigree<br/>Phenotype