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1. PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

2. Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

3. Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder

4. Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder

5. Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.

6. Expanding the phenotype of the X-linked BCOR microphthalmia syndromes

7. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

8. De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.

9. De novo disruption of the proteasome regulatory subunit PSMD12 causes a syndromic neurodevelopmental disorder

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