The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease
Sign Up to like & getrecommendations! Published in 2022 at "BMC Pediatrics"
DOI: 10.1186/s12887-022-03287-1
Abstract: Background Hirschsprung disease (HSCR) is a complex genetic disorder characterized by the lack of ganglion cells in the intestines. A current study showed that the NRG1 rare variant frequency in Indonesian patients with HSCR is… read more here.
Keywords: hrg hrg; impact nrg1; hirschsprung disease; methylation ... See more keywords