Name: Carsten Werner
Academic title: Dipl. rer. nat., PhD
Which is your area of expertise for the "Disease/group of diseases"?
Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):
Gene therapy, genome editing, primary cell culture, flow cytometry, high-performance liquid chromatography
Rare anemia Hemoglobinopathy Beta-thalassemia and related diseases Beta-thalassemia Beta-thalassemia major Beta-thalassemia intermedia Dominant beta-thalassemia Beta-thalassemia associated with another hemoglobin anomaly Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Delta-beta-thalassemia Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin Lepore-beta-thalassemia syndrome Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Sickle cell disease and related diseases Sickle cell anemia Sickle cell disease associated with an other hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Rare hemolytic anemia
|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Molecular Genetics Thalassaemia Department||Τμήμα Μοριακής Γενετικής Θαλασσαιμίας||Red blood cell defects||Cyprus Institute of Neurology and Genetics (CING)|