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Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study
Chaudhary, Spandan, Dhawan, Dipali, Bagali, Prashanth G., S.Chaudhary, Pooja, Chaudhary, Abhinav, Singh, Sanjay, Vudathala, SrinivasVolume:
7
Language:
english
Journal:
Molecular Genetics and Metabolism Reports
DOI:
10.1016/j.ymgmr.2016.04.002
Date:
June, 2016
File:
PDF, 214 KB
english, 2016