APA

Hahn K., Pollmann L., Nowak J., Nguyen A. H. H., Haake K., Neehus A., Waqas S. F. H., Pessler F., Baumann U., Hetzel M., Casanova J., Schulz A., Bustamante J., Ackermann M. & Lachmann N. (2020). Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency. : Molecular therapy. Methods & clinical development.

Chicago

Hahn Katharina, Pollmann Liart, Nowak Juliette, Nguyen Ariane Hai Ha, Haake Kathrin, Neehus Anna-Lena, Waqas Syed F Hassnain, Pessler Frank, Baumann Ulrich, Hetzel Miriam, Casanova Jean-Laurent, Schulz Ansgar, Bustamante Jacinta, Ackermann Mania and Lachmann Nico. 2020. Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency. : Molecular therapy. Methods & clinical development.

Harvard

Hahn K., Pollmann L., Nowak J., Nguyen A. H. H., Haake K., Neehus A., Waqas S. F. H., Pessler F., Baumann U., Hetzel M., Casanova J., Schulz A., Bustamante J., Ackermann M. and Lachmann N. (2020). Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency. : Molecular therapy. Methods & clinical development.

MLA

Hahn Katharina, Pollmann Liart, Nowak Juliette, Nguyen Ariane Hai Ha, Haake Kathrin, Neehus Anna-Lena, Waqas Syed F Hassnain, Pessler Frank, Baumann Ulrich, Hetzel Miriam, Casanova Jean-Laurent, Schulz Ansgar, Bustamante Jacinta, Ackermann Mania and Lachmann Nico. Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency. : Molecular therapy. Methods & clinical development. 2020.