Gene expression profiling in patients with Idiopathic Achalasia
Ontology highlight
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
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