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Bellus, Gary A.

https://orcid.org/0000-0001-7492-3324

A5071396644 | I4210096275

Clinical Genetics and Genomic Medicine, Geisinger, 100 N. Academy Ave., Danville, PA 17822, USA

Citations 2

Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer

Science Advances | January 22, 2020 | Volume: 6 | Issue: 4 | Pages: No page available

10.1126/sciadv.aax0021 | PMID 32010779

Two lysine acyltransferases govern histone H3 propionylation at lysine 23 in normal and pathological conditions.

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation

Human Mutation | July 14, 2015 | Volume: 36 | Issue: 11 | Pages: 1052-1063

10.1002/humu.22832 | PMID 26178382