Cargando…
Investigation of Genetic Mutations in High-risk and Low-risk Basal Cell Carcinoma in a Non-Caucasian Population by Whole Exome Sequencing
This study analysed genomic mutations in basal cell carcinoma using whole exome sequencing of DNA specimens obtained from 20 Korean patients. Histological evaluation determined that 15 (75%) were low-risk basal cell carcinomas, and 5 (25%) were high-risk basal cell carcinomas. Seventy-five percent o...
Autores principales: | KIM, Hyun Jee, LEE, Minho, LEE, Young Bok, YU, Dong Soo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Publication of Acta Dermato-Venereologica
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367048/ https://www.ncbi.nlm.nih.gov/pubmed/33928395 http://dx.doi.org/10.2340/00015555-3820 |
Ejemplares similares
-
Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype
por: Lucariello, Mario, et al.
Publicado: (2016) -
Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia
por: Marshall, Christian R., et al.
Publicado: (2015) -
Genetic Investigation of Bisphosphonate-Related Osteonecrosis of Jaw
(BRONJ) via Whole Exome Sequencing and Bioinformatics
por: Kim, Jee-Hwan, et al.
Publicado: (2015) -
Exome sequence analysis of Kaposiform hemangioendothelioma:
identification of putative driver mutations
por: Egashira, Sho, et al.
Publicado: (2016) -
Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse
por: Sun, Miao, et al.
Publicado: (2012)