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Glucose-6-phosphate dehydrogenase Aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemia

dc.contributor.authorCosta, Elísio
dc.contributor.authorCabeda, José
dc.contributor.authorVieira, Emília
dc.contributor.authorPinto, Rui
dc.contributor.authorPereira, Susana
dc.contributor.authorFerraz, Leonor
dc.contributor.authorSantos, Rosário
dc.contributor.authorBarbot, José
dc.date.accessioned2008-02-15T11:43:26Z
dc.date.available2008-02-15T11:43:26Z
dc.date.issued2000
dc.description.abstractGlucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked enzyme abnormality. The clinical phenotype is variable but often predictable from the molecular lesion. Class I variants (the most severe forms of the disease) cluster within exon 10, in a region that, at the protein level, is believed to be involved in dimerization. Here we describe a de novo mutation (C269Y) of a new class I variant (G6PD Aveiro) that maps to exon 8. Mutant and normal alleles were found in both hematopoietic and buccal cells, indicating the presence of mosaicism. The available model of the protein predicts that this lesion lies in proximity to the dimer interface of the molecule. A possible mechanism to explain the severity of the defect is proposed.en
dc.identifier.citationCosta, Elísio; Cabeda, José; Vieira, Emília; Pinto, Rui; Pereira, Susana; Ferraz, Leonor; Santos, Rosário; Barbot, José (2000). Glucose-6-phosphate dehydrogenase Aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemia. Blood. ISSN 1528-0020. 95:4, p. 1499-1501en
dc.identifier.issn1528-0020
dc.identifier.urihttp://hdl.handle.net/10198/484
dc.language.isoengen
dc.publisherThe American Society of Hematologyen
dc.subjectG6PDen
dc.subjectAveiroen
dc.titleGlucose-6-phosphate dehydrogenase Aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemiaen
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccess
rcaap.typearticleen

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