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Ita Margaretha Nainggolan

Research Fellow

Qualification:

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

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Publications

  1. 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.
    PubMed
  2. 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.
    PubMed
  3. 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.
    PubMed
  4. Alpha thalassaemia in Indonesia: phenotypes and molecular defects.
    Adv Exp Med Biol. 2003;531:47-56.
    PubMed
  5. The hemoglobin O mutation in Indonesia: distribution and phenotypic expression.
    J Hum Genet. 2001;46(9):499-505.
    PubMed