Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening

Background. Beta thalassemia is one of the most common hereditary disorders worldwide. In Iran, it is frequently reported from northern and southern provinces. In order to prevent child birth to be affected by this complication, prenatal screening and diagnosis are carried out nationwide. However, i...

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Detalles Bibliográficos
Autores principales: Mahdavi, Mohammad Reza, Karami, Hosein, Akbari, Mohammad Taghi, Jalali, Hosein, Roshan, Payam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639694/
https://www.ncbi.nlm.nih.gov/pubmed/23662220
http://dx.doi.org/10.1155/2013/906292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639694/
https://www.ncbi.nlm.nih.gov/pubmed/23662220
http://dx.doi.org/10.1155/2013/906292

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