A genome-wide DNA methylation signature for SETD1B-related syndrome

Overview of attention for article published in Clinical Epigenetics, November 2019

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🔬 "A genome-wide DNA methylation signature for SETD1B-related syndrome", I. Madrigal, R. Rabionet, M. Alders et al. #RecercaCRAIBiologiaUB 👉Article: https://t.co/xr1WdMyrqz (open access) https://t.co/x5ZpGIUJKc

SETD1B mutations cause #epilepsy and #intellectual_disability, and lead to a specific methylation pattern, as shown by the latest manuscript of which I am co-author @geneticsUB. https://t.co/WTse91tMhg

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