Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome
Abstract Background Gorlin-Goltz syndrome (GS) is an inherited disease characterized by predisposition to basal cell carcinomas (BCCs) and various developmental defects, whose numerous disease-causing PTCH1 mutations have been identified in the hedgehog (Hh) signaling pathway. Methods In this study,...
Main Authors: | Lihua Ye, Li Wang, Kexin Peng, Ou Fang, Zhen Tian, Caihua Li, Xiaopeng Fu, Qingdong Chen, Jia Chen, Jing Luan, Zhenghua Zhang, Qiaoan Zhang |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2022-08-01
|
Series: | BMC Medical Genomics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12920-022-01324-7 |
Similar Items
-
Gorlin Goltz Syndrome- A Rare Disease Reported In Bangladesh
by: Nafisa Afroze, et al.
Published: (2022-10-01) -
Gorlin–Goltz Syndrome: A Case Report and Literature Review with <i>PTCH1</i> Gene Sequencing
by: Hyo Seong Kim, et al.
Published: (2023-07-01) -
Gorlin-Goltz syndrome from diagnosis to treatment: Role of the dentist
by: Basma Zaher, et al.
Published: (2023-03-01) -
Gorlin-Goltz Syndrome: Multiple Basal Cell Carcinoma, Bifid Rib, Palmar and Plantar Pits in a 50-Year-Old Woman
by: Emilaine Balatibat, et al.
Published: (2020-05-01) -
Gorlin-goltz syndrome
by: B V Shobha, et al.
Published: (2011-01-01)