Found: 2
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HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis.
- Published in:
- British Journal of Haematology, 2017, v. 177, n. 4, p. 597, doi. 10.1111/bjh.14574
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- Publication type:
- Article
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
- Published in:
- 2019
- By:
- Publication type:
- journal article