A large deletion in the human -globin cluster caused by a replication error is associated with an unexpectedly mild phenotype-Reference-Cited by-同舟云学术

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A large deletion in the human -globin cluster caused by a replication error is associated with an unexpectedly mild phenotype

Published:2008-07-09 Issue:19 Volume:17 Page:3084-3093
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Rugless M. J.,Fisher C. A.,Old J. M.,Sloane-Stanley J.,Ayyub H.,Higgs D. R.,Garrick D.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/19/3084/7072258/ddn205.pdf

Reference39 articles.

1. Long-range regulation of ?? globin gene expression during erythropoiesis

2. Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus

3. A Regulatory SNP Causes a Human Genetic Disease by Creating a New Transcriptional Promoter

4. Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.

5. A novel α-globin gene arrangement in man

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1. Genetic Basis and Molecular Diagnosis of Hemoglobinopathies;Reference Module in Biomedical Sciences;2023

2. Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia;Nature Communications;2017-09-04

3. A Novel 31.1 kb α-Thalassemia Deletion (– –MEX3) Found in a Mexican Family;Hemoglobin;2017-05-04

4. Update in the genetics of thalassemia: What clinicians need to know;Best Practice & Research Clinical Obstetrics & Gynaecology;2017-02

5. Mechanisms underlying structural variant formation in genomic disorders;Nature Reviews Genetics;2016-02-29

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