A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations

Published 2010 View Full Article

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Title
A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF PEDIATRICS
Volume 169, Issue 6, Pages 661-666
Publisher
Springer Nature
Online
2010-02-24
DOI
10.1007/s00431-010-1150-6

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