Microdeletions and mutations of CREBBP (CBP) gene can cause
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Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
RSTS Encyclopedia MDPI
Microdeletions and mutations of CREBBP (CBP) gene can cause
Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
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
Targeted degradation of the enhancer lysine acetyltransferases CBP and p300 - ScienceDirect
Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients