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α-thalassaemia

Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hypochromic anaemia, and a clinical phenotype varying from almost asymptomatic to a lethal haemolytic anaemia. It is probably the most common monogenic gene disorder in the world and is especially freque...

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Detalles Bibliográficos
Autores principales: Harteveld, Cornelis L, Higgs, Douglas R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887799/
https://www.ncbi.nlm.nih.gov/pubmed/20507641
http://dx.doi.org/10.1186/1750-1172-5-13