Further evidence for a genetic basis of haemoglobin H disease from newborn offspring of patients
HAEMOGLOBIN H disease is usually a mild to moderate, sometimes severe, thalassaemic disease, characterized by the presence of haemoglobin (Hb) H in addition to Hb A, and intraerythrocytic inclusion bodies 1-3 . Hb H is usually not detectable in either parent of the patients. The genetic basis of the...
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| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Letter |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/9986 |
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| Institution: | Mahidol University |