Cargando…
Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus
BACKGROUND: Autoimmune Addison’s disease (AAD) is a rare, highly heritable autoimmune endocrinopathy. It is possible that there may be some highly penetrant variants which confer disease susceptibility that have yet to be discovered. METHODS: DNA samples from 23 multiplex AAD pedigrees from the UK a...
Autores principales: | Mitchell, Anna L., Bøe Wolff, Anette, MacArthur, Katie, Weaver, Jolanta U., Vaidya, Bijay, Erichsen, Martina M., Darlay, Rebecca, Husebye, Eystein S., Cordell, Heather J., Pearce, Simon H. S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456164/ https://www.ncbi.nlm.nih.gov/pubmed/26042420 http://dx.doi.org/10.1371/journal.pone.0123550 |
Ejemplares similares
-
Correction: Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus
por: Mitchell, Anna L., et al.
Publicado: (2015) -
The natural history of 21-hydroxylase autoantibodies in autoimmune Addison’s disease
por: Wolff, Anette Boe, et al.
Publicado: (2021) -
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
por: Brønstad, Ingeborg, et al.
Publicado: (2011) -
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans
por: Pazderska, Agnieszka, et al.
Publicado: (2016) -
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease
por: Aslaksen, Sigrid, et al.
Publicado: (2019)