Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?-Reference-Cited by-同舟云学术

Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?

Published:2017-03-31 Issue:3 Volume:81 Page:125-128
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Hariharan Priya¹,Gorivale Manju¹,Colah Roshan¹,Ghosh Kanjaksha²,Nadkarni Anita¹

Affiliation:

1. Department of Haematogenetics; National Institute of Immunohaematology (ICMR); Parel Mumbai India

2. Blood Bank; Surat Raktadan Kendra & Research Centre; Surat Gujarat India

Funder

Indian Council of Medical Research

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ahg.12191/fullpdf

Reference12 articles.

1. Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known c-gene mutations associated with hereditary persistence of fetal haemoglobin;Amato;Int J Lab Hematol,2014

2. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin;Borg;Nat Genet,2010

3. The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity;Chen;BMC Med Genet,2010

4. Application of covalent reverse dot blot hybridization for rapid prenatal diagnosis of the common Indian thalassemia syndromes;Colah;Indian J Hematol Blood Transfus,1997

5. Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal haemoglobin levels in adults;Gallienne;Haematologica,2012

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