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Updated: Oct 1, 2026

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Published on: April 4, 2018
A novel beta0-thalassemia mutation at codon 55 (-A) and a rare 17 bp deletion at codons 126-131 in the Indian
Anita Nadkarni1, Takehisa Sakaguchi, Hiroshi Takaku
1Gene Dynamics Group, Institute of Molecular and Cell Biology, Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan.
Abstract:
A new mutation at codon 55 (-A) and a rare mutation, a 17 bp deletion at codons 126-131, that gives rise to beta0-thalassemia, were found in the Indian population by means of direct sequencing of two polymerase chain reaction products generated from a 2.3 kb DNA fragment containing the whole beta-globin gene. Each polymerase chain reaction product was sequenced on both strands in a mutation-loading format, showing all nucleotide substitutions or deletions/insertions, including mutations and polymorphisms, in the product. The entire protocol requires four sequencing reactions/gel loadings after two successive polymerase chain reactions, which simplifies the mutation search process and reduces the reading error rate.
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