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Autor:
Diclehan Oral, Veysiye Hülya Üzel, Mehmet Akif Çürük, Selda Şimşek, Murat Söker, Selahaddin Tekes
Objectives Hemoglobin disorders are quite heterogeneous in the Turkish population. Up to now, more than forty different beta thalassemia mutations and 60 hemoglobin variants have been characterized in the country. The aim of this study was to investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fdeb65ece4400a20264343b1d1b73b1
https://doi.org/10.1515/tjb-2020-0546
https://doi.org/10.1515/tjb-2020-0546