Article

Exploring Pathway Interactions to Detect Molecular Mechanisms of Disease: 22q11.2 Deletion Syndrome

2022-10-10

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold> 22q11.2 Deletion Syndrome (22q11DS) is a genetic disorder characterized by the deletion of adjacent genes at a location specified as q11.2 of chromosome 22, resulting in an array of clinical phenotypes including autistic spectrum disorder, schizophrenia, congenital heart defects, and immune deficiency. Many characteristics of the disorder are known, such as the p...

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Literature Corpus work: 79b971ef-db02-510f-ac84-ad51540c1281
DOI: 10.21203/rs.3.rs-2093258/v1

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