The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. Yilmaz, S. & Sedat Yilmaz Hemoglobin, 43(3):174–181, August, 2019. MAG ID: 2968433087doi abstract bibtex Abstractβ-Thalassemia (β-thal) is the most common hereditary genetic blood disorder. The aims of this study were: (i) to determine the mutation types and the frequency of these mutations in β-thal ...
@article{yilmaz_spectrum_2019,
title = {The {Spectrum} of β-{Thalassemia} {Mutations} in {Siirt} {Province}, {Southeastern} {Turkey}.},
volume = {43},
doi = {10.1080/03630269.2019.1647852},
abstract = {Abstractβ-Thalassemia (β-thal) is the most common hereditary genetic blood disorder. The aims of this study were: (i) to determine the mutation types and the frequency of these mutations in β-thal ...},
number = {3},
journal = {Hemoglobin},
author = {Yilmaz, Sedat and {Sedat Yilmaz}},
month = aug,
year = {2019},
doi = {10.1080/03630269.2019.1647852},
pmid = {31411089},
note = {MAG ID: 2968433087},
pages = {174--181},
}
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