Ita Margaretha Nainggolan

Research Fellow


  • S.Si. (Padjajaran University)
  • M.Biomed in medical biology (University of Indonesia)
  • PhD in medical biology (University of Indonesia)



  • Severe alpha-thalassemia intermedia due to a compound heterozygosity for the highly unstable Hb Adana (HBA2: c.179G>A) and a novel codon 24 (HBA2: c.75T>A) mutation. Hemoglobin. 2014;38(2):149-51. doi: 10.3109/03630269.2013.863206. Epub 2013 Dec 18.
  • Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional alpha(+)-thalassemia mutations: diverse hematological and clinical features. Hemoglobin. 2013;37(3):297-305. doi: 10.3109/03630269.2013.775149. Epub 2013 Apr 25.
  • Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)]. Hemoglobin. 2010;34(4):394-401. doi: 10.3109/03630269.2010.493405.
  • Alpha thalassaemia in Indonesia: phenotypes and molecular defects. Adv Exp Med Biol. 2003;531:47-56.
  • The hemoglobin O mutation in Indonesia: distribution and phenotypic expression. J Hum Genet. 2001;46(9):499-505.