Cargando…
Novel Variations in the KDM5C Gene Causing X-Linked Intellectual Disability
BACKGROUND AND OBJECTIVES: To investigate the pathogenicity of 2 novel KDM5C variations, report the clinical and neuroimaging findings, and review the available literature. METHODS: Physical examinations, structural neuroimaging studies, and exome sequence analysis were performed. KDM5C constructs w...
Autores principales: | Wu, Po-Ming, Yu, Wen-Hao, Chiang, Chi-Wu, Wu, Chen-Yu, Chen, Jia-Shing, Tu, Yi-Fang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641966/ https://www.ncbi.nlm.nih.gov/pubmed/34877407 http://dx.doi.org/10.1212/NXG.0000000000000646 |
Ejemplares similares
-
Comorbidities associated with genetic abnormalities in children with intellectual disability
por: Chen, Jia-Shing, et al.
Publicado: (2021) -
Human X-linked Intellectual Disability Factor CUL4B Is Required for Post-meiotic Sperm Development and Male Fertility
por: Lin, Chien-Yu, et al.
Publicado: (2016) -
Chromatin Sensing by the Auxiliary Domains of KDM5C Regulates Its Demethylase Activity and Is Disrupted by X-linked Intellectual Disability Mutations
por: Ugur, Fatima S., et al.
Publicado: (2023) -
A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family
por: Wu, Shaomin, et al.
Publicado: (2022) -
Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability
por: Sanchis-Juan, Alba, et al.
Publicado: (2019)