dc.creatorOjeda, Mara Jorgelina
dc.creatorPerez, Susana M.
dc.creatorCalvo, Karina Lucrecia
dc.creatorPratti, Arianna F.
dc.creatorVoss, María E.
dc.creatorMilani, Angela Cristina
dc.creatorChiappe, Gustavo
dc.creatorErramouspe, Beatriz
dc.creatorBragós, Irma M.
dc.date.accessioned2016-06-09T16:11:35Z
dc.date.accessioned2018-11-06T13:29:54Z
dc.date.available2016-06-09T16:11:35Z
dc.date.available2018-11-06T13:29:54Z
dc.date.created2016-06-09T16:11:35Z
dc.date.issued2013-01
dc.identifierOjeda, Mara Jorgelina; Perez, Susana M.; Calvo, Karina Lucrecia; Pratti, Arianna F.; Voss, María E.; et al.; Hemoglobin Interlaken in combination with beta thalassemia trait; PAGEPress®; Thalassemia Reports; 3; 1; 1-2013; 11-12
dc.identifier2039-4365
dc.identifierhttp://hdl.handle.net/11336/6123
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1876025
dc.description.abstractWe report a rare a1 globin gene variant (Hb Interlaken) found in a 63-year-old woman of Italian ancestry living in Buenos Aires Province, Argentina. The variant, a missense mutation at cd15 (GGT → GAT) causing a Gly →Asp amino acid substitution and also known as Hb J Oxford, was found in combination with the common thalassemia trait cd 39 (C→T). The clinical picture of the patient was that of a b-thalassemia trait.
dc.languageeng
dc.publisherPAGEPress®
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.pagepressjournals.org/index.php/thal/article/view/625
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.4081/thal.2013.e3
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/10.4081/thal.2013.e3
dc.rightshttps://creativecommons.org/licenses/by-nc/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTHALASSEMIA
dc.subjectHEMOGLOBINOPATHIES
dc.subjectMICROCYTIC HYPOCROMIC ANEMIA
dc.subjectHB INTERLAKEN
dc.titleHemoglobin Interlaken in combination with beta thalassemia trait
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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