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Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (–T) at codon 69 in association with IVS 1-5 (G>C) mutation

✍ Scribed by R. Angalena; S. Aggarwal; S. R. Phadke; A. Dalal


Book ID
114897886
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
154 KB
Volume
34
Category
Article
ISSN
1751-5521

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