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Article

Spectrum of α-thalassemia mutations including first observation of - -(FIL) deletion in Hatay Province, Turkey.

Blood cells, molecules & diseases - 1 Jun 2013

Celik Muhammet Murat, Gunesacar Ramazan, Oktay Gonul, Duran Gulay Gulbol, Kaya Hasan

Abstract excerpt

Alpha thalassemia (α-thal) is one of the most common genetic disorders in the world. It is characterized by the absence or reduced expression of α-globin genes. The frequency of α-thal mutations in the province of Hatay in South Turkey is unknown. Therefore, in the present study, we aimed to investigate the spectrum of α-thal mutations in this province. Three hundred and nine patients were tested for α-thal...

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Identifiers

PMID: 23419704
DOI: 10.1016/j.bcmd.2013.01.012

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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