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
Read MoreIBG Rare and Undiagnosed Diseases Platform Member Dr. Kasim Diril’s group published a study on Rahman Syndrome in FEBS Open Bio
Read MoreOn January 13, 2024, between 12.45-16.15, a half-day hybrid meeting titled “Variants of Uncertain Clinical Significance (VUS) in Pediatric Neurology
Read MoreWe are pleased to announce an upcoming seminar featuring Prof. Dr. Ahmet Özen, a leading expert in the field of
Read MoreAs part of the RareBoost project, “Rare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop” was held
Read MoreWithin the scope of the RareBoost ERA Chair project supported by the European Union H2020 program at Izmir Biomedicine and
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