Cargando…
Mosaicism and incomplete penetrance of PCDH19 mutations
BACKGROUND: Mutations in the PCDH19 gene have mainly been reported in female patients with epilepsy. To date, PCDH19 mutations have been reported in hundreds of females and only in 10 mosaic male epileptic patients with mosaicism. OBJECTIVE: We aimed to investigate the occurrence of mosaic PCDH19 mu...
Autores principales: | Liu, Aijie, Yang, Xiaoxu, Yang, Xiaoling, Wu, Qixi, Zhang, Jing, Sun, Dan, Yang, Zhixian, Jiang, Yuwu, Wu, Xiru, Wei, Liping, Zhang, Yuehua |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581080/ https://www.ncbi.nlm.nih.gov/pubmed/30287595 http://dx.doi.org/10.1136/jmedgenet-2017-105235 |
Ejemplares similares
-
Postzygotic mosaicism in cerebral cavernous malformation
por: Rath, Matthias, et al.
Publicado: (2020) -
A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome
por: Bar, Daniel Z, et al.
Publicado: (2017) -
PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency
por: Chen, Yi, et al.
Publicado: (2022) -
Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort
por: Yang, Xiaoxu, et al.
Publicado: (2017) -
Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome
por: Xu, Xiaojing, et al.
Publicado: (2015)