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New WHO classification of genetic variants causing G6PD deficiency.
Luzzatto, Lucio; Bancone, Germana; Dugué, Pierre-Antoine; Jiang, Weiying; Minucci, Angelo; Nannelli, Caterina; Pfeffer, Daniel; Prchal, Josef; Sirdah, Mahmoud; Sodeinde, Olugbemiro; Vulliamy, Tom; Wanachiwanawin, Wanchai; Cunningham, Jane; Bosman, Andrea.
Afiliação
  • Luzzatto L; Department of Hematology, University of Florence, Piazza San Marco, 4 - 50121Firenze, Italy.
  • Bancone G; Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Thailand.
  • Dugué PA; School of Clinical Sciences at Monash Health, Monash University, Melbourne, Australia.
  • Jiang W; Department of Medical Genetics and Bioinformatics, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
  • Minucci A; Departmental Unit of Molecular and Genomic Diagnostics, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Nannelli C; Department of Experimental and Clinical Medicine, University of Florence, Firenze, Italy.
  • Pfeffer D; Global and Tropical Health Division, Menzies School of Public Health, Darwin, Australia.
  • Prchal J; Department of Medicine, University of Utah, Salt Lake City, United States of America.
  • Sirdah M; Biology Department, Al Azhar University-Gaza, Gaza, occupied Palestinian territory, including east Jerusalem.
  • Sodeinde O; Department of Paediatrics, University of Ibadan, Ibadan, Nigeria.
  • Vulliamy T; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom of Great Britain and Northern Ireland.
  • Wanachiwanawin W; Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Cunningham J; Global Malaria Programme, World Health Organization, Geneva, Switzerland.
  • Bosman A; Global Malaria Programme, World Health Organization, Geneva, Switzerland.
Bull World Health Organ ; 102(8): 615-617, 2024 Aug 01.
Article em En | MEDLINE | ID: mdl-39070600
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Organização Mundial da Saúde / Deficiência de Glucosefosfato Desidrogenase Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Organização Mundial da Saúde / Deficiência de Glucosefosfato Desidrogenase Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article