Perez-Sanchez, Inmaculada <br/><br/>
Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance.  [electronic resource] 

 -  Current gene therapy  2018 
 - 246-251 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1875-5631 
<br/><br/><label>Standard No.: </label>10.2174/1566523218666180709125346  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged, 80 and over<br/>Carrier Proteins--genetics<br/>Child, Preschool<br/>Dystrophin--genetics<br/>Female<br/>G Protein-Coupled Inwardly-Rectifying Potassium Channels--genetics<br/>Humans<br/>Male<br/>Muscular Dystrophy, Duchenne--genetics<br/>Mutation<br/>Penetrance<br/>Phenotype<br/>Prognosis<br/>Sequence Deletion