Effects of SEMA3 polymorphisms in Hirschsprung disease patients.

. GunadiAkhmad MakhmudiNunik Agustrianinull Rochadi

Published in: Pediatric surgery international (2016)

SEMA3 rs12707682 and rs1583147 variants are not common risk factors for HSCR in Indonesia. The rarity of the SEMA3 rs11766001 polymorphism in Indonesian population might be due to a founder effect.

Keyphrases

end stage renal disease
newly diagnosed
ejection fraction
chronic kidney disease
peritoneal dialysis
copy number
gene expression
dna methylation
patient reported