A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period

被引：0
|
作者：
Florian Gundel
Stefan Eber
Axel Heep
机构：
[1] Harlaching Hospital,Department of Paediatrics
来源：
Annals of Hematology | 2011年 / 90卷
关键词：
Hereditary Spherocytosis; Germ Cell Line; Transfusion Independence; Affected Infant; Osmotic Resistance;
D O I：
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中图分类号：
学科分类号：
摘要：
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页码：231 / 232
页数：1
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