Findlay, Andrew R <br/><br/>
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy.  [electronic resource] 

 -  Neuromuscular disorders : NMD  08 2018 
 - 675-679 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1873-2364 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2018.05.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Humans<br/>Male<br/>Muscle Weakness--genetics<br/>Muscle, Skeletal--pathology<br/>Muscular Diseases--genetics<br/>Mutation, Missense<br/>Myosin Heavy Chains--genetics