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Microdeletions and mutations of CREBBP (CBP) gene can cause

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Last updated 06 julho 2024

Microdeletions and mutations of CREBBP (CBP) gene can cause

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

Microdeletions and mutations of CREBBP (CBP) gene can cause

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

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

Frontiers Cornelia de Lange Syndrome as Paradigm of Chromatinopathies

KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia

Genes, Free Full-Text

PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.

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

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

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

KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia

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