Microdeletions and mutations of CREBBP (CBP) gene can cause

Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients - Spena - 2015 - Clinical Genetics - Wiley Online Library

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics

New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Microdeletions and mutations of CREBBP (CBP) gene can cause

The Lysine Acetyltransferases in Cardiovascular Disease

Microdeletions and mutations of CREBBP (CBP) gene can cause

The transcriptional coactivator and histone acetyltransferase CBP regulates neural precursor cell development and migration, Acta Neuropathologica Communications

PHD fi nger mutations in CBP in Rubinstein – Taybi patients. ( A ) DGGE

Schematic representation of mouse CBP. Amino acid residues 1 and 2441

Frontiers Impaired Regulation of Histone Methylation and Acetylation Underlies Specific Neurodevelopmental Disorders

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease - ScienceDirect

The transcriptional coactivator and histone acetyltransferase CBP regulates neural precursor cell development and migration, Acta Neuropathologica Communications

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics