Common genetic polymorphisms at three loci affect HbF levels in β-thalassemia patients from Southern China.

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Blood Cells, Molecules & Diseases

• Publication date

  2016-11-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.bcmd.2016.10.019PMID 27835778
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Thalassaemia.

  2012cited by this paper
• A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.

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• MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13

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• Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

  2010cited by this paper
• A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E

  2009cited by this paper
• BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.

  2008cited by this paper
• Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

  2008cited by this paper
• Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific Repressor BCL11A

  2008cited by this paper

• No citing papers are available for this paper.