Congenital neutropenia in a newborn

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Congenital neutropenia comprises a variety of genetically heterogeneous phenotypic traits. Molecular elucidation of the underlying genetic defects has yielded important insights into the physiology of neutrophil differentiation and function. Non-syndromic variants of congenital neutropenia are caused by mutations in ELA2, HAX1, GFI1, or WAS. Syndromic variants of congenital neutropenia may be d...

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ژورنال

عنوان ژورنال: Journal of Perinatology

سال: 2011

ISSN: 0743-8346,1476-5543

DOI: 10.1038/jp.2010.166