Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations
| Autor: | Germeshausen, Manuela, Grudzien, Magda, Zeidler, Cornelia, Abdollahpour, Hengameh, Yetgin, Sevgi, Rezaei, Nima, Ballmaier, Matthias, Grimbacher, Bodo, Welte, Karl *, Klein, Christoph |
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| Zdroj: | In Blood 15 May 2008 111(10):4954-4957 |
| Databáze: | ScienceDirect |
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