Li, Liting <br/><br/>
JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome.  [electronic resource] 

 -  PloS one  2015 
 - e0130355 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0130355  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alagille Syndrome--genetics<br/>Asian People--genetics<br/>Base Sequence<br/>Calcium-Binding Proteins--genetics<br/>Child<br/>China<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Intercellular Signaling Peptides and Proteins--genetics<br/>Jagged-1 Protein<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation--genetics<br/>Receptors, Notch--metabolism<br/>Sequence Analysis, DNA<br/>Serrate-Jagged Proteins