Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease.

@article{Lee2016AssociationAO,
  title={Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease.},
  author={Jin Sol Lee and J T Oh and Jeong Hyun Kim and Jeong-Meen Seo and Dae Yeon Kim and Kwi-Won Park and Hyun-Young Kim and Kyuwhan Jung and Byung Park and Insong Koh and Hyoung Doo Shin},
  journal={Journal of pediatric gastroenterology and nutrition},
  year={2016},
  volume={62 1},
  pages={64-70}
}
PURPOSE Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder, which is caused by no neuronal ganglion cells in part or all of distal gastrointestinal tract. Recently, our genome-wide association study has identified solute carrier family 6, proline IMINO transporter, member 20 (SLC6A20) as one of the potential risk factors for HSCR… CONTINUE READING