Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective

OBJECTIVE: Alpha thalassemia syndromes are caused by mutations on one or more of the four α-globin genes. Mutations could be either more commonly deletional or non-deletional. As some deletions (3.7 and 4.2) cause α+-thalassemia, some cause (-20.5, MED, THAI, FIL) α0 -thalassemia. The aim of this st...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Turk J Haematol
Egile Nagusiak: Karakaş, Zeynep, Koç, Begüm, Temurhan, Sonay, Elgün, Tuğba, Karaman, Serap, Asker, Gamze, Gençay, Genco, Timur, Çetin, Yıldırmak, Zeynep Yıldız, Celkan, Tiraje, Devecioğlu, Ömer, Aydın, Filiz
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Galenos Publishing 2015
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4805326/
https://ncbi.nlm.nih.gov/pubmed/26377141
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjh.2014.0204
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