RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas

Familial PHEOs (pheochromocytomas) are inherited as an autosomal dominant trait, and inherited PHEOs can be one clinical phenotype of clinical syndromes, such as multiple endocrine neoplasia type 2A (MEN2A). In recent years, there has been a lot of controversy about the factors affecting the penetra...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Lin, Yang, Kun-Qi, Fan, Peng, Gong, Ding-Xu, Zhang, Lin, Lu, Yi-Ting, Meng, Xu, Zhou, Xian-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140906/
https://www.ncbi.nlm.nih.gov/pubmed/35627249
http://dx.doi.org/10.3390/genes13050864

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140906/
https://www.ncbi.nlm.nih.gov/pubmed/35627249
http://dx.doi.org/10.3390/genes13050864

Ejemplares similares