Elucidating the spectrum of alpha thalassemia mutations in iran


12-Sep-2017 06:54

Hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency in certain area particularly Mediterranean and Middle Eastern countries.

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The present study aimed to determine the prevalence of microcytosis among neonates who born in Tehran, Iran.Intellectual disability (ID) is a neuro-developmental disorder which causes considerable socio-economic problems.Some ID individuals are also affected by ataxia, and the condition includes different mutations affecting several genes.....Yousef Shafeghati 1 , Fariba Afroozan 2 , Navid Almadani 2 , Ghazal Vakili 1 1-Genetics Research Center, University of Welfare Sciences & Rehabilitation, Tehran, Iran 2-Kariminejad - Najmabadi Pathology & Genetics Center, Tehran Iran Genetics in the 3rd millennium, Vol.

Mahsa Fadaee Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran Kariminejad Najmabadi Pathology and Genetics Center, Tehran, Iran Neuromuscul Disord 7-82. This interval contains more than 40 genes, none of which has been implicated in MR so far.Fifty six (16.2%) patients had minor β-thalassemia.



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