Cargando…
Over-representation of the G12S polymorphism of the SDHD gene in patients with MEN2A syndrome
OBJECTIVE: To evaluate whether germline variants of the succinate dehydrogenase genes might be phenotypic modifiers in patients with multiple endocrine neoplasia type 2. Mutations of genes encoding subunits of the succinate dehydrogenase are associated with hereditary paraganglioma/pheochromocytoma...
Autores principales: | Lendvai, Nikoletta, Tóth, Miklos, Valkusz, Zsuzsanna, Bekő, Gabriella, Szücs, Nikolette, Csajbók, Éva, Igaz, Péter, Kriszt, Balázs, Kovács, Balázs, Rácz, Károly, Patócs, Attila |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328831/ https://www.ncbi.nlm.nih.gov/pubmed/22584711 http://dx.doi.org/10.6061/clinics/2012(Sup01)15 |
Ejemplares similares
-
True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome
por: Kövesdi, Annamária, et al.
Publicado: (2019) -
Differentially Expressed miRNAs Influence Metabolic Processes in Pituitary Oncocytoma
por: Krokker, Lilla, et al.
Publicado: (2019) -
Tissue miRNA Combinations for the Differential Diagnosis of Adrenocortical Carcinoma and Adenoma Established by Artificial Intelligence
por: Turai, Péter István, et al.
Publicado: (2022) -
Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
por: Igaz, Ivan, et al.
Publicado: (2015) -
Integrative analysis of neuroblastoma and pheochromocytoma genomics data
por: Szabó, Peter M, et al.
Publicado: (2012)