Liao, Xin <br/><br/>
Rare RNF213 variants and the risk of intracranial artery stenosis/occlusion disease in Chinese population: a case-control study.  [electronic resource] 

 -  BMC medical genetics  03 2019 
 - 55 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2350 
<br/><br/><label>Standard No.: </label>10.1186/s12881-019-0788-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Adult<br/>Aged<br/>Asian People--genetics<br/>Case-Control Studies<br/>China<br/>Exome<br/>Female<br/>Genetic Testing<br/>Genetic Variation<br/>Heterozygote<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Male<br/>Middle Aged<br/>Phenotype<br/>Sequence Analysis, DNA--methods<br/>Ubiquitin-Protein Ligases--genetics<br/>Vertebrobasilar Insufficiency--genetics