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Journal Articles

Homozygous calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency

Alexandre P. A. Theocharides, Pontus Lundberg, Asvin K. K. Lakkaraju, Veronika Lysenko, Renier Myburgh, Adriano Aguzzi, Radek C. Skoda, Markus G. Manz
Journal: Blood
Blood (2016) 127 (25): 3253–3259.
https://doi.org/10.1182/blood-2016-02-696310
Published: 2016
Includes: Supplemental data
Journal Articles

Romano M, Dri P, Dadalt L, Patriarca P, Baralle FE. Biochemical and molecular characterization of hereditary myeloperoxidase deficiency. Blood . 1997;90(10): 4126-4134 .

Journal: Blood
Blood (2013) 121 (25): 5104.
https://doi.org/10.1182/blood-2013-05-502021
Published: 2013
Journal Articles

Biochemical and Molecular Characterization of Hereditary Myeloperoxidase Deficiency

Maurizio Romano, Pietro Dri, Liviana Dadalt, Pierluigi Patriarca, Francisco E. Baralle
Journal: Blood
Blood (1997) 90 (10): 4126–4134.
https://doi.org/10.1182/blood.V90.10.4126
Published: 1997
Journal Articles

Aberrant restriction endonuclease digests of DNA from subjects with hereditary myeloperoxidase deficiency

WM Nauseef
Journal: Blood
Blood (1989) 73 (1): 290–295.
https://doi.org/10.1182/blood.V73.1.290.290
Published: 1989
Journal Articles

Posttranslational processing of a human myeloid lysosomal protein, myeloperoxidase

WM Nauseef
Journal: Blood
Blood (1987) 70 (4): 1143–1150.
https://doi.org/10.1182/blood.V70.4.1143.1143
Published: 1987