Naom, I <br/><br/>
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Oct 1998 
 - 495-501 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/s0960-8966(98)00065-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Biopsy<br/>Brain--diagnostic imaging<br/>Child<br/>DNA Mutational Analysis<br/>Electrophysiology<br/>Family Health<br/>Female<br/>Humans<br/>Laminin--genetics<br/>Magnetic Resonance Imaging<br/>Male<br/>Muscles--innervation<br/>Muscular Dystrophies--diagnosis<br/>Pedigree<br/>Point Mutation<br/>Radionuclide Imaging