Association of Neuregulin 1 rs7835688  G  >  C, rs16879552 T  >  C and rs2439302 G  >  C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung's Disease.

Conclusions: Our findings suggested that NRG1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C polymorphisms are not a risk factor in development of HSCR. PMID: 31738640 [PubMed - as supplied by publisher]
Source: Fetal and Pediatric Pathology - Category: Pathology Tags: Fetal Pediatr Pathol Source Type: research