Homozygosity for the Severe β + -Thalassemia Mutation [IVS-I-5 (G>C)] Causes the Phenotype of Thalassemia Trait: An Extremely Rare Presentation

Author： Bohara Vinaykumar Raut Lalit Badarkhe Girish Roy Siddartha S. Chaudhuri Utpal

Publisher： Informa Healthcare

ISSN： 0363-0269

Source： Hemoglobin, Vol.37, Iss.1, 2013-02, pp. : 101-105

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