Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia

被引：11
|
作者：
Lanciotti, Marina [1 ]
Indaco, Stefania [1 ]
Bonanomi, Sonia [2 ]
Coliva, Tiziana [2 ]
Mastrodicasa, Elena [3 ]
Caridi, Gianluca [4 ]
Calvillo, Michaela [1 ]
Dufour, Carlo [1 ]
机构：
[1] G Gaslini Inst Children, Dept Pediat Hematooncol, Hematol Lab, Genoa, Italy
[2] Univ Milano Bicocca, San Gerardo Hosp, Pediat Clin, Monza, Italy
[3] S Maria della Misericordia Hosp, Unit Pediat Oncol & Haematol, Perugia, Italy
[4] G Gaslini Childrens Hosp, Lab Pathophysiol Uremia, Genoa, Italy
来源：
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷 / 01期
关键词：
D O I：
10.3324/haematol.2009.015370
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：168 / 169
页数：2
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