Effect of semaphorin 3C gene variants in multifactorial Hirschsprung disease.

. GunadiFiko RyantonoRaman Sethinull Marcellus Alvin Santoso KalimPriscillia ImeldaDevy MelatiSusan SimanjayaWilliam WiditjiarsoRirid Tri PitakaNur ArfianKristy IskandarAkhmad MakhmudiPoh-San Lai

Published in: The Journal of international medical research (2021)

This is the first comprehensive report of SEMA3C screening in patients of Asian ancestry with HSCR and identifies rs1527482 as a possible disease risk allele in this population.

Keyphrases

end stage renal disease
copy number
genome wide
ejection fraction
newly diagnosed
chronic kidney disease
prognostic factors
patient reported outcomes
dna methylation