Microdeletions and mutations of CREBBP (CBP) gene can cause
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RSTS Encyclopedia MDPI
From Whole Gene Deletion to Point Mutations of EP300‐Positive Rubinstein–Taybi Patients: New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks - Negri - 2016 - Human Mutation - Wiley Online Library
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
KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Microdeletions and mutations of CREBBP (CBP) gene can cause
Microdeletions and mutations of CREBBP (CBP) gene can cause
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
Frontiers Cornelia de Lange Syndrome as Paradigm of Chromatinopathies
CBP deficiency leads to HMT-mediated epigenetic modification. Induction
Genes, Free Full-Text
Fourteen causative CREBBP mutations detected by direct sequencing.
High frequency of mosaic CREBBP deletions in Rubinstein–Taybi syndrome patients and mapping of somatic and germ-line breakpoints - ScienceDirect
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