Microdeletions and mutations of CREBBP (CBP) gene can cause

Molecular insight into CREBBP and TANGO2 variants causing intellectual disability - Hussain - The Journal of Gene Medicine - Wiley Online Library

Fourteen causative CREBBP mutations detected by direct sequencing.

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

Human CREBBP acetyltransferase is impaired by etoposide quinone, an oxidative and leukemogenic metabolite of the anticancer drug etoposide through modification of redox-sensitive zinc-finger cysteine residues - ScienceDirect

CREBBP (CREB binding protein)

Microdeletions and mutations of CREBBP (CBP) gene can cause

Genes, Free Full-Text

Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC

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

Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome

High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis

Microdeletions and mutations of CREBBP (CBP) gene can cause

Microdeletions and mutations of CREBBP (CBP) gene can cause

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

Microdeletions and mutations of CREBBP (CBP) gene can cause