A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India.

Waseem ChauhanMohammad AfzalZeeba Zaka-Ur-RabMd Salik Noorani

Published in: The application of clinical genetics (2021)

A total of 108 β-thalassemia alleles were studied from 46 homozygous and 31 compound heterozygous patients. All the individuals were from 20 districts of the Western Uttar Pradesh, India.

Keyphrases

end stage renal disease
ejection fraction
prognostic factors
peritoneal dialysis
south africa