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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:EClinicalMedicine
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7565196/
https://ncbi.nlm.nih.gov/pubmed/33089125
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.eclinm.2020.100528
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados