Glycine

hemoglobin subunit alpha 1 ; Homo sapiens







5 Article(s)
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1 32498570 Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (HBA1: c.179G > A) and Codon 127 (A > T) (HBA2: c.382A > T) in an Iranian Family. 2020 Mar 1
2 28361593 First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok. 2016 Nov 1
3 24933025 Serum and adipose tissue amino acid homeostasis in the metabolically healthy obese. 2014 Jul 3 1
4 23806011 Two complex associations of an HBD mutation and a rare α hemoglobinopathy. 2013 1
5 22738642 Identification of a new HBA1 gene mutation (HBA1:c.301-2A>T) in cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser]. 2012 3