Identification of compound heterozygosity for a rare beta-globin gene mutation, codon 15 (-T) with a common mutation IVS1-5 (G>C) by direct sequencing in a Bangladeshi patient.

Kazi Nadim Hasan, Md. Abdul Khaleque, Ashish Kumar Majumder, Md. Mizanur Rahman, Sharif Akhteruzzaman

This paper is cited by the following papers:
[1] Thalassemia intermedia phenotype resulting from rare combination of c.46delT [Codon15 (‐T)] mutation of beta globin gene and HPFH3