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...

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Detalles Bibliográficos
Autores principales: Van, Lily, Heung, Tracy, Malecki, Sarah L., Fenn, Christian, Tyrer, Andrea, Sanches, Marcos, Chow, Eva W.C., Boot, Erik, Corral, Maria, Dash, Satya, George, Susan R., Bassett, Anne S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565196/
https://www.ncbi.nlm.nih.gov/pubmed/33089125
http://dx.doi.org/10.1016/j.eclinm.2020.100528

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565196/
https://www.ncbi.nlm.nih.gov/pubmed/33089125
http://dx.doi.org/10.1016/j.eclinm.2020.100528

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