Cargando…
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Chromatin remodeling is of crucial importance during brain development. Pathogenic alterations of several chromatin remodeling ATPases have been implicated in neurodevelopmental disorders. We describe an index case with a de novo missense mutation in CHD3, identified during whole genome sequencing o...
Ejemplares similares
-
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
por: Blok, Lot Snijders, et al.
Publicado: (2019) -
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
por: Snijders Blok, Lot, et al.
Publicado: (2019) -
Estimates of the prevalence of speech and motor speech disorders in
persons with complex neurodevelopmental disorders
por: Shriberg, Lawrence D., et al.
Publicado: (2019) -
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
por: Worthey, Elizabeth A, et al.
Publicado: (2013) -
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental Disorder
por: Calpena, Eduardo, et al.
Publicado: (2019)