- Title
- A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major alpha-Globin Regulatory Element (MCS-R2) and alpha(0)-Thalassemia
- Creators - without role
- Lv-Yin Huang - College Station Medical CenterJin-Mei Yan - College Station Medical CenterJian-Ying Zhou - College Station Medical CenterJian Li - College Station Medical CenterXing-Mei Xie - Guangzhou Medical UniversityDong-Zhi Li - College Station Medical CenterJianying Zhou - ISTD Pillar
- Publication Details
- Acta haematologica, Vol.138(1), pp.61-64
- Publisher
- Karger
- Number of pages
- 4
- Grant note
- 81571448 / National Natural Science Foundation of China; National Natural Science Foundation of China (NSFC) 2016A020215218 / Guangdong Provincial Department of Science and Technology Agency
- Identifiers
- 9911759609846
- Academic Unit
- ISTD Pillar
- Language
- English
- Resource Type
- Journal article
Journal article
A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major alpha-Globin Regulatory Element (MCS-R2) and alpha(0)-Thalassemia
Acta haematologica, Vol.138(1), pp.61-64
01/08/2017
PMID: 28743121
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