Cargando…
The chromosome 6q22.33 region is associated with age at diagnosis of type 1 diabetes and disease risk in those diagnosed under 5 years of age
AIMS/HYPOTHESIS: The genetic risk of type 1 diabetes has been extensively studied. However, the genetic determinants of age at diagnosis (AAD) of type 1 diabetes remain relatively unexplained. Identification of AAD genes and pathways could provide insight into the earliest events in the disease proc...
Autores principales: | Inshaw, Jamie R. J., Walker, Neil M., Wallace, Chris, Bottolo, Leonardo, Todd, John A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719131/ https://www.ncbi.nlm.nih.gov/pubmed/28983737 http://dx.doi.org/10.1007/s00125-017-4440-y |
Ejemplares similares
-
Prenatally detected six duplications at Xp22.33-p11.22: a case report
por: Zhang, Xue, et al.
Publicado: (2023) -
Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population
por: Pereda, Celia M, et al.
Publicado: (2015) -
Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate
por: Szalai, Renata, et al.
Publicado: (2023) -
Turner syndrome due to Xp22.33 deletion with preserved gonadal function: case report
por: D’Ambrosio, Fabiola, et al.
Publicado: (2019) -
Common Variants at 9q22.33, 14q13.3, and ATM Loci, and Risk of Differentiated Thyroid Cancer in the French Polynesian Population
por: Maillard, Stéphane, et al.
Publicado: (2015)