Gene expression profiling in patients with Idiopathic Achalasia

ABSTRACT: Comparison of gene expression profiles in 12 resected specimens from achalasia, a rare motility disorder characterized manometrically by the absence of peristalsis and an incompletely relaxing lower esophageal sphincter (LES), patients with those from 5 controls to identify critical genes and highly perturbed pathways with potential involvement in achalasia

ORGANISM(S): Homo sapiens

SUBMITTER: Massimo Carella 

PROVIDER: E-MTAB-3962 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress