A novel G6PC3 homozygous 1-bp deletion as a cause of severe congenital neutropenia
Abstract
To the editor:
Hereditary severe congenital neutropenia (SCN) represents a heterogeneous group of diseases characterized by early-onset life-threatening bacterial infections associated with absolute neutrophil counts (ANC) below 500/μL.[1][1],[2][2] In recent years, different studies...
Paper Details
Title
A novel G6PC3 homozygous 1-bp deletion as a cause of severe congenital neutropenia
Published Date
Aug 20, 2009
Journal
Volume
114
Issue
8
Pages
1718 - 1719
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Notes
History