Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia-Reference-Cited by-同舟云学术

Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia

Published:2014-10-31 Issue:10 Volume:9 Page:e110740
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Sheehan Vivien A.,Crosby Jacy R.,Sabo Aniko,Mortier Nicole A.,Howard Thad A.,Muzny Donna M.,Dugan-Perez Shannon,Aygun Banu,Nottage Kerri A.,Boerwinkle Eric,Gibbs Richard A.,Ware Russell E.,Flanagan Jonathan M.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference31 articles.

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3. Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?;DR Powars;Blood,1984

4. The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up;MH Steinberg;Am J Hematol,2010

5. The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS);E Voskaridou;Blood,2010

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