Cargando…
A novel compound-heterozygous EPCAM mutation in congenital tufting enteropathy
Autores principales: | Zhao, Ruiqin, Yang, Fan, Chen, Xinggu, Fu, Haiyan, Li, Guigui, Cheng, Lijuan, Li, Xiaolei |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710291/ https://www.ncbi.nlm.nih.gov/pubmed/36457962 http://dx.doi.org/10.5114/aoms/155185 |
Ejemplares similares
-
New mutation in EPCAM for congenital tufting enteropathy: A case report
por: Zhou, Yan-Qiong, et al.
Publicado: (2020) -
EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome
por: Pathak, Sagar J., et al.
Publicado: (2018) -
New Mutations of EpCAM Gene for Tufting Enteropathy in Saudi Arabia
por: AlMahamed, Shaden, et al.
Publicado: (2017) -
Three Novel EPCAM Variants Causing Tufting Enteropathy in Three Families
por: Ayyıldız Civan, Hasret, et al.
Publicado: (2021) -
Long-Term Follow-Up of Tufting Enteropathy Caused by EPCAM Mutation p.Asp253Asn and Absent EPCAM Expression
por: Ozler, Oğuz, et al.
Publicado: (2020)