Microdeletions and mutations of CREBBP (CBP) gene can cause

Microdeletions and mutations of CREBBP (CBP) gene can cause

Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

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

Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4

Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

IJMS, Free Full-Text

CREB-binding Protein - an overview

Microdeletions and mutations of CREBBP (CBP) gene can cause