Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A T<sup>Indian</sup>(AATA<i>AA</i>>AATA– –) Mutation in Four Indian Families-Reference-Cited by-同舟云学术

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Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A T^Indian(AATAAA>AATA– –) Mutation in Four Indian Families

Published:2013-03-21 Issue:3 Volume:37 Page:277-284
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Nair Sona B.,Nadkarni Anita H.,Ghosh Kanjaksha,Colah Roshan B.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.774284

Reference19 articles.

1. The Alpha Thalassaemias

2. Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

3. Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia

4. α-thalassaemia

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1. Molecular Heterogeneity of Hb H Disease in India;Thalassemia Reports;2022-07-06

2. The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center;International Journal of Laboratory Hematology;2018-11-29

3. CRISPR/Cas9-mediated mutation of tyrosinase (Tyr) 3′ UTR induce graying in rabbit;Scientific Reports;2017-05-08

4. Diagnostic pitfalls of less well recognized HbH disease;Blood Cells, Molecules, and Diseases;2015-12

5. Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses;Hemoglobin;2015-11-16

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