Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease
- PMID: 20864588
- DOI: 10.1182/blood-2010-04-281345
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources

