22q11.2 microdeletion and increased risk for type 2 diabetes

22q11.2 microdeletion and increased risk for type 2 diabetes

Background: The 22q11.2 microdeletion is the pathogenic copy number variation (CNV) associated with 22q11.2 deletion syndrome (22q11.2DS, formerly known as DiGeorge syndrome). Familiar endocrinological manifestations include hypoparathyroidism and hypothyroidism, with recent elucidation of elevated...

Full description

Bibliographic Details
Main Authors: Lily Van, Tracy Heung, Sarah L. Malecki, Christian Fenn, Andrea Tyrer, Marcos Sanches, Eva W.C. Chow, Erik Boot, Maria Corral, Satya Dash, Susan R. George, Anne S. Bassett
Format: Article
Language:English
Published: Elsevier 2020-09-01
Series:EClinicalMedicine
Subjects:
Diabetes
Genetics
Risk
Structural variant
Molecular diagnostics
Early diagnosis
Online Access:http://www.sciencedirect.com/science/article/pii/S2589537020302728

Internet

http://www.sciencedirect.com/science/article/pii/S2589537020302728

Similar Items