The spectrum of rare and novel indel mutations responsible for β Thalassemia in eastern India
Sajan Sinha, Atanu Kumar Dutta, Paramita Bhattacharya, Subham Bhattacharya, Mrinal Kanti Das
The paper identifies rare and novel indel mutations in β Thalassemia patients in eastern India using molecular methods and highlights the limitations of HPLC screening.
Indian Journal of Clinical Biochemistry · Jan 3, 2023Peer-reviewedGenetic & Genomic Medicine