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

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

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