Literature DB >> 27829299

Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon.

Gift D Pule1, Valentina J Ngo Bitoungui2, Bernard Chetcha Chemegni2, Andre P Kengne3, Ambroise Wonkam1.   

Abstract

High level of Hb F has been shown to improve survival in sickle cell disease. Among 453 Cameroonians with sickle cell disease, we have investigated 18 selected single-nucleotide polymorphisms (SNPs) in novel and suggestive loci associated with Hb F level identified through a genomewide association study in sickle cell disease patients in Tanzania, and whole-genome sequencing of a population from Sardinia. Seven of 10 variants reported in Sardinians were either monomorphic or very rare in the Cameroonians. No associations were observed with any SNPs and Hb F levels in Cameroonians affected by sickle cell disease. The present study illustrates the complexity of replicating Hb F-promoting variants association results across populations.

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Keywords:  Cameroon; Hb F; Sardinia; Tanzania; sickle cell disease

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Year:  2016        PMID: 27829299     DOI: 10.1080/03630269.2016.1251453

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  2 in total

1.  Genetic variants in the G gamma-globin promoter modulate fetal hemoglobin expression in the Colombian population.

Authors:  Cristian Fong; Yesica Mendoza; Guillermo Barreto
Journal:  Genet Mol Biol       Date:  2020-04-22       Impact factor: 1.771

2.  Genetic research and clinical analysis of deletional Chinese Gγ+(Aγδβ)0 -thalassemia and Southeast Asian HPFH in South China.

Authors:  Yuanjun Wu; Qianyu Yao; Ming Zhong; Jianying Wu; Longxu Xie; Linnan Su; Fubing Yu
Journal:  Ann Hematol       Date:  2020-09-15       Impact factor: 3.673

  2 in total

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