Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma

BACKGROUND: Basan syndrome is a rare autosomal-dominant ectodermal dysplasia with certain clinic-pathological features caused by mutations in the SMARCAD1 gene. Currently, no skin malignancy related to Basan syndrome has been reported. This study was aimed at identifying related gene mutations in a...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiong, Ying, Chen, Ting, Yu, Jia, Zhou, He, Lu, Baozhen, Chen, Lijie, Sun, Liwei, Wang, Can, Li, Sujun, Wu, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113868/
https://www.ncbi.nlm.nih.gov/pubmed/35592705
http://dx.doi.org/10.1155/2022/7840710

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113868/
https://www.ncbi.nlm.nih.gov/pubmed/35592705
http://dx.doi.org/10.1155/2022/7840710

Ejemplares similares