1966
DOI: 10.1016/0009-8981(66)90187-2
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Hemoglobin Agenogi (α2β290lys), a slow-moving hemoglobin of a Japanese family resembling Hb-E

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1967
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Cited by 46 publications
(4 citation statements)
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“…Variant hemoglobin was strongly suspected from the dissociation between IA-HbA1c and HPLC-SM-HbA1c in this case. Analysis of the globin gene revealed a heterozygous mutation at β codon 90 of Glu (GAG) → Lys (AAG) and the patient was diagnosed with Hb Agenogi [11].…”
Section: Resultsmentioning
confidence: 99%
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“…Variant hemoglobin was strongly suspected from the dissociation between IA-HbA1c and HPLC-SM-HbA1c in this case. Analysis of the globin gene revealed a heterozygous mutation at β codon 90 of Glu (GAG) → Lys (AAG) and the patient was diagnosed with Hb Agenogi [11].…”
Section: Resultsmentioning
confidence: 99%
“…1d). As Hb Agenogi is slow-moving variant hemoglobin [11], HPLC-VM-HbA1c is more likely to produce a correct value. HPLC-VM-HbA1c measured using 4 different instruments was 6.4 ± 0.2% (mean ± SD).…”
Section: Resultsmentioning
confidence: 99%
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“…Although external, there is no involvement of the side chain in α 1 β 1 contacts and it is not clear how the mutation alters O 2 affinity. Surprisingly, the conservative mutation of glutamic to aspartic acid produces an increased oxygen affinity in Hb Pierre–Benite, while the gross charge changes associated with Glu→Lys and Glu→Gly β90 mutations led to small decreases in affinity in Hbs Agenogi and Roseau‐Pointe‐a‐Pitre, respectively (Miyaji et al ., 1966; Merault et al ., 1985). Baklouti et al .…”
Section: Resultsmentioning
confidence: 99%