A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia-Reference-Cited by-同舟云学术

A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia

Published:2014-02 Issue:2 Volume:89 Page:187-193
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Belfer Inna¹,Youngblood Victoria²,Darbari Deepika S.²³,Wang Zhengyuan²,Diaw Lena²,Freeman Lita⁴,Desai Krupa²,Dizon Michael²,Allen Darlene⁴,Cunnington Colin⁵,Channon Keith M.⁵,Milton Jacqueline⁶,Hartley Stephen W.⁶,Nolan Vikki⁷,Kato Gregory J.⁴,Steinberg Martin H.⁶,Goldman David⁸,Taylor James G.²

Affiliation:

1. Department of Anesthesiology; University of Pittsburgh School of Medicine; Pittsburgh Pennsylvania

2. Genomic Medicine Section; Hematology Branch, NHLBI, NIH; Bethesda Maryland

3. Division of Pediatric Hematology; Center for Cancer and Blood Disorders, Children's National Medical Center; Washington DC

4. Sickle Cell Vascular Disease Section; Hematology Branch, NHLBI, NIH; Bethesda Maryland

5. Department of Cardiovascular Medicine; John Radcliffe Hospital, University of Oxford; Oxford United Kingdom

6. Center of Excellence in Sickle Cell Disease and Department of Medicine; Boston University School of Medicine; Boston Massachusetts

7. School of Public Health, University of Memphis; Memphis Tennessee

8. Laboratory of Neurogenetics; NIAAA, NIH; Bethesda Maryland

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23613/fullpdf

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3. Mortality in sickle cell disease. Life expectancy and risk factors for early death;Platt;N Engl J Med,1994

4. Are there clinical phenotypes of homozygous sickle cell disease?;Alexander;Br J Haematol,2004

5. The search for genetic modifiers of disease severity in the beta-hemoglobinopathies;Lettre;Cold Spring Harb Perspect Med,2012

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