Xiao, Yatao <br/><br/>
Loss of mitochondrial protein CHCHD10 in skeletal muscle causes neuromuscular junction impairment.  [electronic resource] 

 -  Human molecular genetics  07 2020 
 - 1784-1796 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddz154  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Agrin--pharmacology<br/>Animals<br/>Disease Models, Animal<br/>Gene Expression Regulation--drug effects<br/>Humans<br/>Mice<br/>Mice, Knockout<br/>Mitochondria--genetics<br/>Mitochondrial Proteins--genetics<br/>Motor Neurons--metabolism<br/>Muscle, Skeletal--metabolism<br/>Neuromuscular Junction--drug effects<br/>Neuromuscular Junction Diseases--genetics<br/>Receptors, Cholinergic--genetics<br/>Synapses--genetics<br/>Synaptic Transmission--genetics