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pro vyhledávání: '"Sandip Hirapara"'
Autor:
Niraj Sojitra, Spandan Chaudhary, Dipali Dhawan, Sandip Hirapara, Khyati Chandratre, Arpita Ghosh, Prashanth G. Bagali, Sanjay Singh
Publikováno v:
Clinical & Medical Biochemistry Open Access.
Co-inheritance of sickle cell anemia and β-thalassemia traits require medical attention. Individuals with sickle cell and β-thalassemia disorders produce abnormal form of hemoglobin or decreased synthesis or complete absence of the β-globin chains