Potential association between ITPKC genetic variations and Hirschsprung disease
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DOI: 10.1007/s11033-017-4111-6
Abstract: Hirschsprung disease (HSCR) is a congenital and complex disorder characterized by intestinal obstruction due to the absence of enteric neurons along variable lengths of the hindgut. Our recent genome-wide association study (GWAS) has revealed regional… read more here.
Keywords: hirschsprung disease; association; potential association; itpkc ... See more keywords