Condition: Decreased peristalsis


rs1057516046 in ACTG2 gene and Decreased peristalsis PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs1557043622 in SLC35A2 gene and Decreased peristalsis PMID 30817854 2019 SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals.