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Hemoglobin ; 48(2): 133-137, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38632978

RESUMEN

The first identification of a novel α1-Globin variant, Hb Ormylia in 11 Greeks originating from a small village, Ormylia, Chalkidiki, Greece is reported. The new genetic variant leads to the production of a hemoglobin variant that can be identified and quantified by High-Performance Liquid Chromatography. Capillary and classic electrophoresis were not informative. Direct DNA sequencing revealed a new mutation C > G mutation at codon 21 of α1 gene (His > Gln). The new variant has been named Hb Ormylia and this is the first description of this genetic variant of α1 gene in the literature.


Asunto(s)
Hemoglobinas Anormales , Globinas alfa , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Globinas alfa/genética , Talasemia alfa/genética , Talasemia alfa/diagnóstico , Sustitución de Aminoácidos , Grecia , Hemoglobinas Anormales/genética , Mutación
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