Cherry, Smita <br/><br/>
Charcot-Marie-Tooth 2B mutations in rab7 cause dosage-dependent neurodegeneration due to partial loss of function.  [electronic resource] 

 -  eLife  Dec 2013 
 - e01064 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2050-084X 
<br/><br/><label>Standard No.: </label>10.7554/eLife.01064  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Charcot-Marie-Tooth Disease--genetics<br/>Disease Models, Animal<br/>Drosophila<br/>Guanosine Diphosphate--metabolism<br/>Guanosine Triphosphate--metabolism<br/>Laminopathies<br/>Molecular Sequence Data<br/>Mutation<br/>Neurodegenerative Diseases--genetics<br/>Sensory Receptor Cells--metabolism<br/>Sequence Homology, Nucleic Acid<br/>rab GTP-Binding Proteins--chemistry<br/>rab7 GTP-Binding Proteins