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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Indian J Hematol Blood Transfus
Hlavní autoři: Yuregir, Ozge Ozalp, Ayaz, Akif, Yalcintepe, Sinem, Canbek, Sezin, Acik, Didar Yanardag, Yilmaz, Basak Taburoglu, Balci, Tugce B.
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer India 2015
Témata:
Short Communication
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky