Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders

Autor:	Patiroglu, T., Eke Gungor, H., Triop, A., Ekrem UNAL
Předmět:	nervous system macromolecular substances
Zdroj:	Scopus-Elsevier
Popis:	Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders: Severe congenital neutropenia (SCN) is a lire primary myelopoiesis disorder, characterized by reduced absolute neutrophil counts from birth, increased susceptibility to recurrent and life-threatening infections, and a preleukemic predisposition.
Databáze:	OpenAIRE
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