Compound heterozygote of Hb D(Iran) [HBB: c.67G>C, β 22(B4) Glu>Gln] with β(0)-thalassemia [cds 41/42 (-CTTT)] from Eastern India

Lignende værker

• Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)(0)-thalassemia in eastern India
  af: Dehury, Snehadhini, et al.
  Udgivet: (2015)
• Inheritance of Hereditary Persistence of Fetal Haemoglobin (HPFH) in a Family of Western Odisha, India
  af: Patel, Siris, et al.
  Udgivet: (2015)
• Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia
  af: Nasouhipur, Hengameh, et al.
  Udgivet: (2014)
• Influence of Sickle Cell Gene on the Allelic Diversity at the msp-1 locus of Plasmodium falciparum in Adult Patients with Severe Malaria
  af: Patel, Dilip Kumar, et al.
  Udgivet: (2015)
• Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia
  af: Moassas, Faten, et al.
  Udgivet: (2019)