Detection of α-Thalassemia by Using Multiplex Ligation-Dependent Probe Amplification as an Additional Method for Rare Mutations in Southern Turkey

α-thalassemia is the most common single gene disorder in the Cukurova Region in Turkey. It is therefore routinely screened, including premaritally, in our region. The heterogeneous molecular basis of the disease makes α-thalassemia mutation detection difficult and complex. Besides well established m...

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Publicat a:Indian J Hematol Blood Transfus
Autors principals: Yuregir, Ozge Ozalp, Ayaz, Akif, Yalcintepe, Sinem, Canbek, Sezin, Acik, Didar Yanardag, Yilmaz, Basak Taburoglu, Balci, Tugce B.
Format: Artigo
Idioma:Inglês
Publicat: Springer India 2015
Matèries:
Short Communication
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5074955/
https://ncbi.nlm.nih.gov/pubmed/27812256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-015-0617-z
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