Author:
Al-Jamea Lamiaa H.,Woodman Alexander,M. Heiba Nihal,Elshazly Shereen A.,Ben Khalaf Noureddine,Al-Yami Fatimah S.,Bilal Waheed Khawaja,Al Mutair Abbas,Alsedi Ahmad,Quiambao Jenifer V.,Alzahrani Faisal M.,Albaqami Walaa F.,Al Qahtani Faisal H.,Mohammed Aljarah Nasser,Fathallah Dahmani M.,Halim Deifalla Abdel
Subject
Genetics,General Medicine
Reference25 articles.
1. First Observation of two TMPRSS6 gene mutations (G603R and K636AFSX17) in Turkish population;Akisin;Int. J. Blood Res. Disord.,2019
2. Al-Jamea, L.H., Woodman, A., Heiba, N.M., Elshazly, S.A., Khalaf, N.B., Fathallah, D.M., Deifalla, A.H., 2021. Genetic analysis of TMPRSS6 gene in Saudi female patients with iron deficiency anemia. Hematol./Oncol. Stem Cell Ther. 14(1), 41–50.
3. A novel TMPRSS6 mutation that prevents protease auto-activation causes IRIDA;Altamura;Biochem. J.,2010
4. TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia;An;Hum. Mol. Genet.,2012
5. Common variants in TMPRSS6 are associated with iron status and erythrocyte volume;Benyamin;Nat. Genet.,2009
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