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Novel Point Mutation of the α2-Globin Gene ( HBA2 ) and a Rare 2.4 kb Deletion of the α1-Globin Gene ( HBA1 ), Identified in Two Chinese Patients with Hb H Disease

✍ Scribed by So, Chi-Chiu; Chan, Amy Y. Y.; Ma, Edmond S. K.


Book ID
127019938
Publisher
Informa plc
Year
2014
Tongue
English
Weight
895 KB
Volume
38
Category
Article
ISSN
0363-0269

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