Cargando…
Novel Point Mutation of EBSS Gene Coexisted with 1p36 Deletion
EBSS (epidermolysis bullosa simplex superficialis) is mainly caused by gene mutations which targeted protein as plakophilin1, desmoplakin and keratins. 1p36 gene deleted could cause typical clinical manifestations and might also affect the expression of functional genes in other regions. Here we rep...
Autores principales: | Zheng, Yue, Xu, Qingfang, Lai, Wei |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Dermatological Association; The Korean Society for Investigative Dermatology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460473/ https://www.ncbi.nlm.nih.gov/pubmed/34616129 http://dx.doi.org/10.5021/ad.2021.33.5.463 |
Ejemplares similares
-
Endogenous leptin promotes autophagy in EBSS-induced PFCs
por: Jiao, Deling, et al.
Publicado: (2019) -
Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report
por: Yang, Huanhuan, et al.
Publicado: (2023) -
Analysis of p16 gene deletion and point mutation in breast carcinoma.
por: Quesnel, B., et al.
Publicado: (1995) -
A Novel Case of Biliary Atresia in a Premature Neonate With 1p36 Deletion Syndrome
por: Chawla, Vonita, et al.
Publicado: (2018) -
1p36 deletion syndrome: an update
por: Jordan, Valerie K, et al.
Publicado: (2015)