Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.
- DOI
- 10.3324/haematol.2010.029389
- Published
- 2010 Dec
- Container
- Haematologica
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3324/haematol.2010.029389,
title = {Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.},
author = {Rohr J and Beutel K and Maul-Pavicic A and Vraetz T and Thiel J and Warnatz K and Bondzio I and Gross-Wieltsch U and Schündeln M and Schütz B and Woessmann W and Groll AH and Strahm B and Pagel J and Speckmann C and Janka G and Griffiths G and Schwarz K and zur Stadt U and Ehl S},
year = {2010},
journal = {Haematologica},
doi = {10.3324/haematol.2010.029389},
url = {https://doi.org/10.3324/haematol.2010.029389}
}RIS
TY - JOUR TI - Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases. AU - Rohr J AU - Beutel K AU - Maul-Pavicic A AU - Vraetz T AU - Thiel J AU - Warnatz K AU - Bondzio I AU - Gross-Wieltsch U AU - Schündeln M AU - Schütz B AU - Woessmann W AU - Groll AH AU - Strahm B AU - Pagel J AU - Speckmann C AU - Janka G AU - Griffiths G AU - Schwarz K AU - zur Stadt U AU - Ehl S PY - 2010 JO - Haematologica DO - 10.3324/haematol.2010.029389 UR - https://doi.org/10.3324/haematol.2010.029389 ER -
APA
J, R., K, B., A, M., T, V., J, T., K, W., I, B., U, G., M, S., B, S., W, W., AH, G., B, S., J, P., C, S., G, J., G, G., K, S., U, Z. S., & S, E. (2010). Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.. Haematologica. https://doi.org/10.3324/haematol.2010.029389
Source records
- pubmed · retrieved 2026-09-26T05:01:50.753Z