Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population-Reference-Cited by-同舟云学术

Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population

Published:2012-06-26 Issue:2 Volume:89 Page:160-164
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Italia Khushnooma¹,Sawant Pratibha¹,Surve Reema¹,Wadia Marukh¹,Nadkarni Anita¹,Ghosh Kanjaksha¹,Colah Roshan¹

Affiliation:

1. National Institute of Immunohaematology; Parel; Mumbai; India

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2012.01810.x/fullpdf

Reference15 articles.

1. Frequency of β thalassemia trait and other hemoglobinopathies in northern and western India;Madan;Indian J Hum Genet,2010

2. Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human β-globin gene;Orkin;EMBO J,1985

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

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