Research on Rahman Syndrome delivers a novel tool to study the rare genetic condition
IBG Rare and Undiagnosed Diseases Platform Member Dr. Kasim Diril’s group published a study on Rahman Syndrome in FEBS Open Bio
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Rare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop
As part of the RareBoost project, “Rare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop” was held
Read MoreRare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop
Within the scope of the RareBoost ERA Chair project supported by the European Union H2020 program at Izmir Biomedicine and
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