Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations.
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Bodo Grimbacher | Christoph Klein | Nima Rezaei | M. Ballmaier | C. Klein | K. Welte | N. Rezaei | B. Grimbacher | M. Germeshausen | M. Grudzień | Matthias Ballmaier | Manuela Germeshausen | Karl Welte | Magda Grudzien | Cornelia Zeidler | Hengameh Abdollahpour | Sevgi Yetgin | S. Yetgin | C. Zeidler | H. Abdollahpour
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