Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis-Reference-Cited by-同舟云学术

Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis

Author:

Guan Hongzai¹,Liang Xinping¹,Zhang Rong²,Wang Haiyan³,Liu Wenmiao⁴,Zhang Ru⁴,Yang Jie⁵,Liu Shiguo⁴

Affiliation:

1. Department of Clinical Hematology, The Medical College of Qingdao University, Qingdao, People’s Republic of China

2. Department of Clinical Laboratory, The Qingdao Central Hospital, Qingdao, People’s Republic of China

3. Department of Blood Transfusion, The Affiliated Hospital of Qingdao University, Qingdao, People’s Republic of China

4. Prenatal Diagnosis Center, The Affiliated Hospital of Qingdao University, Qingdao, People’s Republic of China

5. Department of Hematology, The Affiliated Hospital of Qingdao University, Qingdao, People’s Republic of China

Funder

the National Key Research and Development Program of China

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

Reference24 articles.

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