Cargando…
A Novel Germline Pathogenic Variant of RECQL4 Gene in an Iranian Pedigree with Familial Squamous Cell Carcinoma: A Brief Report
Squamous cell carcinoma (SCC) is the most common human solid tumor and the leading cause of cancer death. SCC of the breast is a very rare type of cancer that has not been well researched. Early identification of the genetic factors involved can lead to early diagnosis and targeted treatment. The pr...
Autores principales: | Amin, Mina, Mahmoodi-Khaledi, Elaheh, Narrei, Sina, Zeinalian, Mehrdad |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shiraz University of Medical Sciences
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349162/ https://www.ncbi.nlm.nih.gov/pubmed/37456212 http://dx.doi.org/10.30476/IJMS.2022.94539.2587 |
Ejemplares similares
-
Trends of human brucellosis in Central Iran (2010–2018)
por: Khalilian, Mohammad-Sadegh, et al.
Publicado: (2021) -
Enrichment of heterozygous germline RECQL4 loss-of-function variants in pediatric osteosarcoma
por: Maciaszek, Jamie L., et al.
Publicado: (2019) -
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
por: Norouzi, Mahnaz, et al.
Publicado: (2021) -
Clinical implications of germline mutations in breast cancer genes: RECQL
por: Bowden, A. Ramsay, et al.
Publicado: (2019) -
Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients
por: Rashid, Muhammad Usman, et al.
Publicado: (2020)