@article{bozdogan_nonsense_2012,
	title = {{NONSENSE} β-{THALASSEMIA} {MUTATION} {AT} {CODON} 37 ({TGG}{\textgreater}{TGA}), {DETECTED} {FOR} {THE} {FIRST} {TIME} {IN} {THREE} {TURKISH} {CASES}},
	volume = {36},
	doi = {10.3109/03630269.2012.662197},
	abstract = {Thalassemias are genetically heterogeneous group of disorders with reduced or absent production of globin. β-Thalassemia major can be caused by homozygosity or compound heterozygosity for β-globin gene mutation. Here we report, for the first time in Turkey, three cases who carry the nonsense β-thalassemia (β-thal) mutation at codon 37 (TGG{\textgreater}TGA; Trp→Stop) causing premature stop codon.},
	number = {3},
	journal = {Hemoglobin},
	author = {Bozdogan, Sevcan Tug and Unsal, Cagatay and Unsal, Cagatay and Erkman, Hakan and Erkman, Hakan and Genc, Ahmet and Yuregir, Ozge Ozalp and Muslumanoglu, Muhammed Hamza and Aslan, Hüseyin and {Huseyin Aslan} and {Huseyin Aslan} and {Huseyin Aslan}},
	month = may,
	year = {2012},
	doi = {10.3109/03630269.2012.662197},
	pmid = {22385009},
	note = {MAG ID: 2148917128},
	pages = {283--288},
}

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