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...

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Detalles Bibliográficos
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:
Original Articles
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

Internet

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

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