miR-938 rs2505901 T>C Polymorphism Increases Hirschsprung Disease Risk: A Case–Control Study of Chinese Children
Open Access
- 11 November 2021
- journal article
- research article
- Published by Taylor & Francis in Personalized Medicine
- Vol. 18 (6) , 551-558
Abstract
Aim: To explore the association between miR-938 rs2505901 T>C polymorphism and Hirschsprung disease (HSCR) risk in Chinese children. Materials & Methods: We conducted a case–control study in a Chin... Lay abstract Hirschsprung disease (HSCR) is the most common intestinal disorder in infants. Genetic defects play important roles in the occurrence and development of HSCR. This case–control study w...Keywords
Funding Information
- Natural Science Foundation of Guangdong Province, China (2019A1515010971)
- Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease (2019B030301004)
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