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Hemoglobin Kenitraα2β269 (E13) Gly→Arg. A newβVariant of Elevated Expression Associated withα-Thalassemia, Found in a Moroccan Woman

 

作者: DelanoeJ.,   ArousN.,   BlouquitY.,   HafsiaR.,   BardakdjianJ.,   LacombeC.,   RosaJ.,   GalacterosF.,  

 

期刊: Hemoglobin  （Taylor Available online 1985）
卷期: Volume 9, issue 1  

页码: 1-9

 

ISSN:0363-0269

 

年代: 1985

 

DOI:10.3109/03630268508996977

 

出版商: Taylor&Francis

 

数据来源: Taylor

 

摘要:

Hemoglobin Kenitra is a new variant of theβchainα2β269 (E13) Gly→Arg which does not produce any clinical symptoms. It is a slow-moving hemoglobin with a distinctive pattern of electrophoretic mobilities. The stability test was negative. Oxygen affinity studies were not performed. It was found in association withα-thalassemia and microcytosis, but paradoxically a high expression of the variant (55%) was observed.

 

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