(PDF) Identification of de novo EP300 and PLAU variants in a
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The impact of rare germline variants on human somatic mutation
Neurodevelopmental disease genes implicated by de novo mutation
Targeting de novo loss-of-function variants in constrained disease
PDF) Massively parallel identification of functionally
Phenotype and genotype in 52 patients with Rubinstein–Taybi
Case report: a Chinese girl like atypical Rubinstein–Taybi
Comparative Analysis of Drug-like EP300/CREBBP Acetyltransferase
DAXX drives de novo lipogenesis and contributes to tumorigenesis
PDF) Recurrent de novo mutations in neurodevelopmental disorders