Cheng, Chih-Ya <br/><br/>
ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18.  [electronic resource] 

 -  Experimental neurology  May 2015 
 - 143-51 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Validation Study 
<br/><br/><label>ISSN: </label>1090-2430 
<br/><br/><label>Standard No.: </label>10.1016/j.expneurol.2015.03.003  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--chemically induced<br/>Age Factors<br/>Animals<br/>Axons--pathology<br/>Cataract--chemically induced<br/>Cornea--abnormalities<br/>Disease Models, Animal<br/>Endoplasmic Reticulum--pathology<br/>Ethylnitrosourea--pharmacology<br/>Eye--pathology<br/>Hypogonadism--chemically induced<br/>Intellectual Disability--chemically induced<br/>Male<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Transgenic<br/>Microcephaly--chemically induced<br/>Microphthalmos--etiology<br/>Mutagenesis--drug effects<br/>Nerve Degeneration--etiology<br/>Optic Atrophy--chemically induced<br/>Optic Nerve Diseases--etiology<br/>Psychomotor Performance--drug effects<br/>Sequence Deletion--genetics<br/>Testis--pathology<br/>Touch Perception--drug effects<br/>rab GTP-Binding Proteins--deficiency