A single‐center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease‐causing genotypes

• Leo Kager,
• Raúl Jimenez‐Heredia,
• Petra Zeitlhofer,
• Wolfgang Novak,
• Sebastian K. Eder,
• Anna Segarra‐Roca,
• Alexandra Frohne,
• Karin Nebral,
• Matthias Haimel,
• René Geyeregger,
• Katharina Roetzer‐Londgin,
• Oskar A. Haas,
• Kaan Boztug

Affiliations

Leo Kager

St. Anna Children's Hospital Medical University of Vienna Vienna Austria

Raúl Jimenez‐Heredia

St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

Petra Zeitlhofer

Labdia Labordiagnostik Vienna Austria

Wolfgang Novak

St. Anna Children's Hospital Medical University of Vienna Vienna Austria

Sebastian K. Eder

St. Anna Children's Hospital Medical University of Vienna Vienna Austria

Anna Segarra‐Roca

St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

Alexandra Frohne

St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

Karin Nebral

Labdia Labordiagnostik Vienna Austria

Matthias Haimel

St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

René Geyeregger

St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

Katharina Roetzer‐Londgin

St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

Oskar A. Haas

St. Anna Children's Hospital Medical University of Vienna Vienna Austria

Kaan Boztug

St. Anna Children's Hospital Medical University of Vienna Vienna Austria