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Diagnosis of hemoglobinopathy and β-thalassemia by 21-Tesla Fourier transform ion cyclotron resonance mass spectrometry

   
@article{ATM28034,
	author = {Jae-Seok Kim and Hyun Sik Kim},
	title = {Diagnosis of hemoglobinopathy and β-thalassemia by 21-Tesla Fourier transform ion cyclotron resonance mass spectrometry},
	journal = {Annals of Translational Medicine},
	volume = {7},
	number = {Suppl 6},
	year = {2019},
	keywords = {},
	abstract = {Hemoglobin is the oxygen-transport protein in red blood cells consisting of four globulins. Human adult hemoglobin A (HbA), containing two identical α-chains (141 amino acids, 15,126.4 Da) and two identical β-chains (146 amino acids, 15,867.2 Da), accounts for around 97% of the total hemoglobin in a normal adult, whereas HbA2, with two α-chains and two delta-chains, accounts for 1.5–3.5% of the total hemoglobin in normal adults. Moreover, the proportions of HbA, HbA2, and HbF can fluctuate during human development from the fetal to adult stage.},
	issn = {2305-5847},	url = {https://atm.amegroups.org/article/view/28034}
}