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Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.
Chaturvedi, Shruti; Bhatnagar, Pallav; Bean, Christopher J; Steinberg, Martin H; Milton, Jaqueline N; Casella, James F; Barron-Casella, Emily; Arking, Dan E; DeBaun, Michael R.
Afiliação
  • Chaturvedi S; Division of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Bhatnagar P; McKusick-Nathans Institute of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD.
  • Bean CJ; Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA.
  • Steinberg MH; Department of Medicine.
  • Milton JN; Department of Pediatrics, and.
  • Casella JF; Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA.
  • Barron-Casella E; Department of Biostatistics, Boston University School of Public Health, Boston, MA.
  • Arking DE; Division of Pediatric Hematology, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD; and.
  • DeBaun MR; Division of Pediatric Hematology, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD; and.
Blood ; 130(5): 686-688, 2017 08 03.
Article em En | MEDLINE | ID: mdl-28584135
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arteriopatias Oclusivas / Variação Genética / Cromossomos Humanos Par 4 / Polimorfismo de Nucleotídeo Único / Epistasia Genética / Dor Aguda / Anemia Falciforme Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Blood Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Tunísia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arteriopatias Oclusivas / Variação Genética / Cromossomos Humanos Par 4 / Polimorfismo de Nucleotídeo Único / Epistasia Genética / Dor Aguda / Anemia Falciforme Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Blood Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Tunísia