Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature 

被引：0
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作者：
Lichun Xie
Zhihao Xing
Changgang Li
Si-xi Liu
Fei-qiu Wen
机构：
[1] Jinan University,The First Affiliated Hospital
[2] Shenzhen Children’s Hospital,Department of Hematology/Oncology
来源：
BMC Medical Genomics | / 14卷
关键词：
ANK1 gene; Case report; Frame shift mutation; Hereditary spherocytosis; Neonate;
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