Traboulsee, Anthony L <br/><br/>
Common genetic etiology between "multiple sclerosis-like" single-gene disorders and familial multiple sclerosis.  [electronic resource] 

 -  Human genetics  06 2017 
 - 705-714 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-017-1784-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Cholestanetriol 26-Monooxygenase--genetics<br/>Exome<br/>Female<br/>Genetic Diseases, Inborn<br/>Humans<br/>Male<br/>Multiple Sclerosis--genetics<br/>Pedigree<br/>Sequence Homology, Amino Acid