Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype.

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Chromatin Remodeling BAF (SWI/SNF) Complexes in Neural Development and Disorders.Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome.Mutational Landscapes and Phenotypic Spectrum of SWI/SNF-Related Intellectual Disability Disorders

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P2860

Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype.

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Heterozygosity for ARID2 loss- ...... Siris syndrome-like phenotype.

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Heterozygosity for ARID2 loss- ...... Siris syndrome-like phenotype.

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Heterozygosity for ARID2 loss- ...... -Siris syndrome-like phenotype

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P2860

PBAF chromatin-remodeling complex requires a novel specificity subunit, BAF200, to regulate expression of selective interferon-responsive genes.

De novo mutations in epileptic encephalopathies

De novo SOX11 mutations cause Coffin-Siris syndrome

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

BAF200 is required for heart morphogenesis and coronary artery development

Mutations in ARID2 are associated with intellectual disabilities.

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.

ATP-dependent chromatin remodeling: genetics, genomics and mechanisms.

Essential role of ARID2 protein-containing SWI/SNF complex in tissue-specific gene expression.

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Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype.

about

P2860

P2860

Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype.

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