Thomson, C E <br/><br/>
The early phenotype associated with the jimpy mutation of the proteolipid protein gene.  [electronic resource] 

 -  Journal of neurocytology  Mar 1999 
 - 207-21 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0300-4864 
<br/><br/><label>Standard No.: </label>10.1023/a:1007024022663  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age Factors<br/>Animals<br/>Apoptosis<br/>Astrocytes--pathology<br/>Biomarkers<br/>Cell Count<br/>Cell Differentiation<br/>Cells, Cultured<br/>Demyelinating Diseases--genetics<br/>In Situ Hybridization<br/>Male<br/>Mice<br/>Mice, Inbred C3H<br/>Mice, Jimpy--genetics<br/>Microscopy, Electron<br/>Myelin Proteolipid Protein--deficiency<br/>Myelin Sheath--pathology<br/>Nerve Tissue Proteins--analysis<br/>Oligodendroglia--pathology<br/>Phenotype<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Spinal Cord--pathology<br/>X Chromosome--genetics