Ge, Ting <br/><br/>
Novel compound heterozygote mutations of TJP2 in a Chinese child with progressive cholestatic liver disease.  [electronic resource] 

 -  BMC medical genetics  01 2019 
 - 18 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2350 
<br/><br/><label>Standard No.: </label>10.1186/s12881-019-0753-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>China<br/>Cholestasis, Intrahepatic--genetics<br/>Female<br/>Heterozygote<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Infant<br/>Maternal Inheritance<br/>Mutation<br/>Paternal Inheritance<br/>Sequence Analysis, DNA--methods<br/>Zonula Occludens-2 Protein--genetics