Chen, Wenji <br/><br/>
Progressive pseudorheumatoid dysplasia with new-found gene mutation of Wntl inducible signaling pathway protein 3.  [electronic resource] 

 -  Pediatric rheumatology online journal  Sep 2018 
 - 55 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1546-0096 
<br/><br/><label>Standard No.: </label>10.1186/s12969-018-0272-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>CCN Intercellular Signaling Proteins--genetics<br/>Female<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Joint Diseases--congenital<br/>Mutation<br/>Signal Transduction--genetics<br/>Young Adult