Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation

• Marini Thian,
• Birgit Hoeger,
• Anton Kamnev,
• Fiona Poyer,
• Sevgi Köstel Bal,
• Michael Caldera,
• Raúl Jiménez-Heredia,
• Jakob Huemer,
• Winfried F. Pickl,
• Miriam Groß,
• Stephan Ehl,
• Carrie L. Lucas,
• Jörg Menche,
• Caroline Hutter,
• Andishe Attarbaschi,
• Loïc Dupré,
• Kaan Boztug

Affiliations

Marini Thian

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Birgit Hoeger

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Anton Kamnev

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Fiona Poyer

St. Anna Children Hospital, Vienna, Austria;

Sevgi Köstel Bal

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Michael Caldera

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria;

Raúl Jiménez-Heredia

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Jakob Huemer

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Winfried F. Pickl

Medical University of Vienna, Vienna, Austria;

Miriam Groß

Institute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Freiburg, Germany;

Stephan Ehl

Institute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Freiburg, Germany;

Carrie L. Lucas

Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA;

Jörg Menche

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria;

Caroline Hutter

St. Anna Children Cancer Research Institute, Vienna, Austria

Andishe Attarbaschi

St. Anna Children Hospital, Vienna, Austria;

Loïc Dupré

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;

Kaan Boztug

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;