Ufartes, Roser <br/><br/>
Sema3a plays a role in the pathogenesis of CHARGE syndrome.  [electronic resource] 

 -  Human molecular genetics  04 2018 
 - 1343-1352 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/ddy045  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>CHARGE Syndrome--genetics<br/>DNA Helicases--genetics<br/>DNA-Binding Proteins--genetics<br/>Disease Models, Animal<br/>Embryo, Nonmammalian<br/>Epigenesis, Genetic<br/>Genetic Complementation Test<br/>HEK293 Cells<br/>Homeobox Protein Nkx-2.5--genetics<br/>Humans<br/>Kallmann Syndrome--genetics<br/>Mutation<br/>Neural Crest--metabolism<br/>Promoter Regions, Genetic<br/>Semaphorin-3A--genetics<br/>Severity of Illness Index<br/>Xenopus laevis