Literature DB >> 701083

Hemoglobin Legnano (alpha2 141 (HC3) Arg replaced by Leu beta2): a new abnormal human hemoglobin with high oxygen affinity.

F Mavilio, M Marinucci, L Tentori, P P Fontanarosa, U Rossi, S Biagiotti.   

Abstract

An abnormal, fast moving hemoglobin was noted in a 34-yr-old male patient living in Legnano (northern Italy) affected with renal failure and iron deficiency anemia, not related to the presence of the Hb variant. Structural studies have demonstrated a previously undescribed amino acid substitution, alpha 141 Arg replaced by Leu. This new variant has been named Hb Legnano, and is characterized by an increased oxygen affinity and a low cooperativity, at least as far as preliminary functional studies carried out on whole blood have indicated. Family studies are reported: three other heterozygous carriers were observed among the relatives of the propositus, all showing a mild polycythemia which, however, does not seem to produce appreciable clinical consequences.

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Year:  1978        PMID: 701083     DOI: 10.3109/03630267809007070

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  2 in total

1.  A new hemoglobin variant, hemoglobin Nunobiki [alpha 141 (HC3) Arg----Cys]. Notable influence of the carboxy-terminal cysteine upon various physico-chemical characteristics of hemoglobin.

Authors:  S Shimasaki
Journal:  J Clin Invest       Date:  1985-02       Impact factor: 14.808

2.  Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family.

Authors:  S Musumeci; G Schilirò; G Pizzarelli; L Tentori; M Marinucci; P P Fontanarosa; G Russo
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

  2 in total

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