Βιβλιογραφική Τεκμηρίωση:
De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobinM Iwate and symptomatic methemoglobinemia since birth. Viana MB, Belisário AR.Rev Bras Hematol Hemoter. 2014 May-Jun;36(3):230-4.
The -alpha3.7 deletion in alpha-globin genes increases the concentration of fetalhemoglobin and hemoglobin A2 in a Saudi Arabian population.Borgio JF, Abdulazeez S, Almandil NB, Naserullah ZA, Al-Jarrash S, Al-Suliman AM, Elfakharay HI, Qaw FS, Alabdrabalnabi FI, Alkhalifah MA, Shakil Akhtar M, Qutub H, Al-Ali AK.Mol Med Rep. 2018 Jan;17(1):1879-1884.
Development of a high-resolution melting method for the detection ofhemoglobin alpha variants. Shih HC, Er TK, Chang TJ, Chang YS, Liu TC, Chang JG.Clin Biochem. 2010 May;43(7-8):671-6.