Status: new
Identifier: PXD079241
HostingRepository: MassIVE
Species: Homo sapiens
Title: EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome-Histone modifications mass spect
Submitter: Maria J Barrero
LabHead: Maria J. Barrero
Description: Histone modifications quantified by mass spectrometry dataset used in: De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity. A. Hnizda, B. Martinez-Delgado et al.