“…The variant haemoglobin was found to be due to a point mutation CAC → TAC of codon 143 of the beta chain and was subsequently published simultaneously by two groups [12,13] and later named Hb Old Dominion/Burton‐on‐Trent [β143 (H21) His → Tyr][14]. Since these initial reports of four individuals from three families, all of whom had an Irish element in their ancestry, two further Anglo‐Celtic cases [15] and one Korean case [16] have been described.…”
Consequently, we propose greater interaction between diabetologists and the laboratory in an attempt to identify these clinically but not biochemically silent variants to achieve a true estimation of the glycaemic control in affected patients.
“…The variant haemoglobin was found to be due to a point mutation CAC → TAC of codon 143 of the beta chain and was subsequently published simultaneously by two groups [12,13] and later named Hb Old Dominion/Burton‐on‐Trent [β143 (H21) His → Tyr][14]. Since these initial reports of four individuals from three families, all of whom had an Irish element in their ancestry, two further Anglo‐Celtic cases [15] and one Korean case [16] have been described.…”
Consequently, we propose greater interaction between diabetologists and the laboratory in an attempt to identify these clinically but not biochemically silent variants to achieve a true estimation of the glycaemic control in affected patients.
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