Cargando…
Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene
BACKGROUND: Patients with pathogenic variants in ZBTB18 present with Intellectual Disability (ID) with frequent co‐occurrence of corpus callosum (CC) anomalies, hypotonia, microcephaly, growth problems and variable facial dysmorphologies. These features illustrate a key role for ZBTB18 in brain deve...
Autores principales: | van der Schoot, Vyne, de Munnik, Sonja, Venselaar, Hanka, Elting, Mariet, Mancini, Grazia M. S., Ravenswaaij‐Arts, Conny M. A., Anderlid, Britt‐Marie, Brunner, Han G., Stevens, Servi J. C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014478/ https://www.ncbi.nlm.nih.gov/pubmed/29573576 http://dx.doi.org/10.1002/mgg3.387 |
Ejemplares similares
-
Understanding the impact of ZBTB18 missense variation on transcription factor function in neurodevelopment and disease
por: Heng, Julian I.‐T., et al.
Publicado: (2022) -
Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome
por: Basson, M. Albert, et al.
Publicado: (2015) -
Growth in CHARGE syndrome: optimizing care with a multidisciplinary approach
por: Dijk, Dieuwerke R, et al.
Publicado: (2019) -
Congenital arch vessel anomalies in CHARGE syndrome: A frequent feature with risk for co-morbidity()()
por: Corsten-Janssen, Nicole, et al.
Publicado: (2016) -
Understanding Behavior in Phelan-McDermid Syndrome
por: Landlust, Annemiek M., et al.
Publicado: (2022)