Pegoraro, Elena <br/><br/>
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Apr 2007 
 - 321-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2007.01.010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Arginine--genetics<br/>Cardiac Myosins--genetics<br/>Child<br/>Family Health<br/>Female<br/>Humans<br/>Infant<br/>Magnetic Resonance Imaging<br/>Male<br/>Microscopy, Electron, Transmission<br/>Middle Aged<br/>Muscle, Skeletal--pathology<br/>Muscular Diseases--classification<br/>Muscular Dystrophy, Emery-Dreifuss--genetics<br/>Mutation<br/>Myosin Heavy Chains--genetics<br/>Myosins--metabolism<br/>RNA, Messenger--metabolism<br/>Reverse Transcriptase Polymerase Chain Reaction--methods<br/>Tryptophan--genetics