CORDIS Project
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The Chrom_Rare project investigates chromatinopathies, a group of rare genetic diseases, by exploring the genetic and epigenetic factors that affect gene expression and chromatin organization. It aims to develop disease models and new diagnostic and therapeutic strategies to improve the understanding and treatment of t…
Chromatinopathies (CPs) are a group of rare genetic diseases, which share clinical features as well as causal genetic alterations, leading to the inactivation of chromatin regulators involved in gene expression control and 3D chromatin organization.
Within the framework of Chrom_Rare, we will focus on a group of clinically well-defined CPs, including Kabuki Syndrome, Charge Syndrome, Rubinstein-Taybi Syndrome and Cornelia de Lange Syndrome.
Although the causative genes for these CPs have been id…
UNIVERSITA DEGLI STUDI DI TRENTO
Partner organizations (coordinator is shown above), with normalized type and CORDIS activity type. Guests see up to 4 partners.
France, Montpellier
Type: University / higher education
Activity type: Higher or Secondary Education Establishments
SME: No
Germany, Wolfenbuttel
Type: SME
Activity type: Private for-profit entities (excluding Higher or Secondary Education Establishments)
SME: Yes
CENTRE HOSPITALIER UNIVERSITAIRE MONTPELLIER
France, Montpellier
Type: Research institute
Activity type: Research Organisations
SME: No
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