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Annals of Human Biology Volume 38, 2011 - Issue 3
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Short Report

SLC40A1 Q248H allele frequencies and associated SLC40A1 haplotypes in three West African population samples

David Albuquerque Department of Life Sciences, University of Coimbra, Portugal
,
Licínio MancoCorrespondence[email protected]
,
Kovana M. Loua Institut National de Santé Publique, Conakry, Republic de Guinée
,
Ana Paula Arez Centro de Malária e outras Doenças Tropicais (CMDT-LA), Instituto de Higiene e Medicina Tropical (IHMT), Universidade Nova de Lisboa, Portugal
,
Maria de Jesus Trovoada Instituto Gulbenkian de Ciência (IGC), Oeiras, Portugal
,
Luís Relvas Department of Hematology, Centro Hospitalar de Coimbra-EPE, Portugal
,
Tamba S. Millimono Department of Haematology, Donka Hospital, Conakry, Republic de Guinée
,
Silvia L. Rath Institut National de Santé Publique, Conakry, Republic de Guinée
,
Dinora Lopes Centro de Malária e outras Doenças Tropicais (CMDT-LA), Instituto de Higiene e Medicina Tropical (IHMT), Universidade Nova de Lisboa, Portugal
,
Fátima Nogueira Centro de Malária e outras Doenças Tropicais (CMDT-LA), Instituto de Higiene e Medicina Tropical (IHMT), Universidade Nova de Lisboa, Portugal
,
Luís Varandas Centro de Malária e outras Doenças Tropicais (CMDT-LA), Instituto de Higiene e Medicina Tropical (IHMT), Universidade Nova de Lisboa, Portugal
,
Manuela Alvarez Department of Life Sciences, University of Coimbra, Portugal
&
M. Letícia Ribeiro Department of Hematology, Centro Hospitalar de Coimbra-EPE, Portugal
 show all
Pages 378-381 | Received 13 Sep 2010, Accepted 15 Nov 2010, Published online: 14 Jan 2011

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Tamba S. Millimono, Kovana M. Loua, Silvia L. Rath, Luis Relvas, Celeste Bento, Mandiou Diakite, Martin Jarvis, Nathalie Daries, Leticia M. Ribeiro, Licínio Manco & Jaspal S. Kaeda. (2012) High Prevalence of Hemoglobin Disorders and Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Republic of Guinea (West Africa). Hemoglobin 36:1, pages 25-37.
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Yvette Lufungulo Bahati, Joris Delanghe, Ghislain Bisimwa Balaluka, Karl Vandepoele, Justin Cikomola Cirhuza, Antoine Sadiki Kishabongo & Jan Philippé. (2022) Ferroportin Q248H mutation was not found to be protective against malaria and anemia in children under 5 years living in South Kivu/Democratic Republic of Congo, an endemic area of Plasmodium infection. Heliyon 8:9, pages e10460.
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James C. Barton, Howard W. WienerRonald T. Acton. (2022) Estimates of West African Ancestry in African Americans Using Alleles of Iron-Related Genes HJV , SLC40A1 , and TFR2 . Genetic Testing and Molecular Biomarkers 26:2, pages 96-102.
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Wanhui Kang, Alexa Barad, Andrew G Clark, Yiqin Wang, Xu Lin, Zhenglong Gu & Kimberly O O'Brien. (2021) Ethnic Differences in Iron Status. Advances in Nutrition 12:5, pages 1838-1853.
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L. Tom Vlasveld, Roel Janssen, Edouard Bardou-Jacquet, Hanka Venselaar, Houda Hamdi-Roze, Hal Drakesmith & Dorine W. Swinkels. (2019) Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features. Pharmaceuticals 12:3, pages 132.
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De-Liang Zhang, Jian Wu, Binal N. ShahKatja C. GreutélaersManik C. GhoshHayden OllivierreXin-zhuan Su, Philip E. Thuma, George Bedu-AddoFrank P. Mockenhaupt, Victor R. Gordeuk & Tracey A. Rouault. (2018) Erythrocytic ferroportin reduces intracellular iron accumulation, hemolysis, and malaria risk. Science 359:6383, pages 1520-1523.
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Ishmael Kasvosve. (2016) The evolutionary adaptation of hemochromatosis associated mutations during the Neolithic. American Journal of Physical Anthropology 162:2, pages 393-394.
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Justin C. Cikomola, Karl Vandepoele, Philippe B. Katchunga, Antoine S. Kishabongo, Elizaveta Y. Padalko, Marijn M. Speeckaert & Joris R. Delanghe. (2016) The association between fructosamine-3 kinase 900C/G polymorphism, transferrin polymorphism and human herpesvirus-8 infection in diabetics living in South Kivu. Acta Tropica 163, pages 14-19.
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Ishmael Kasvosve, Uyapo Tshwenyego, Thato Phuthego, Garesego Koto, Matshediso Zachariah, Naledi G. Nyepetsi & Modisa S. Motswaledi. (2015) Serum ferritin concentration is affected by ferroportin Q248H mutation in Africans. Clinica Chimica Acta 444, pages 257-259.
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Philippe Bianga Katchunga, Marius Baguma, Jean-René M‘Buyamba-Kabangu, Jan Philippé, Michel P. Hermans & Joris Delanghe. (2013) Ferroportin Q248H mutation, hyperferritinemia and atypical type 2 diabetes mellitus in South Kivu. Diabetes & Metabolic Syndrome: Clinical Research & Reviews 7:2, pages 112-115.
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Ishmael Kasvosve. (2013) Effect of ferroportin polymorphism on iron homeostasis and infection. Clinica Chimica Acta 416, pages 20-25.
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Florence Masaisa, Candace Breman, Jean Bosco Gahutu, Joshua Mukiibi, Joris Delanghe & Jan Philippé. (2012) Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating serum hepcidin levels in Rwandese HIV-positive women. Annals of Hematology 91:6, pages 911-916.
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Yvette Lufungulo Bahati, Joris Delanghe, Ghislain Bisimwa, Karl Vandepoele, Justin Cikomola Cirhuza, Antoine Sadiki Kishabongo & Jan Philippe. (2021) Ferroportin Q248H Mutation is Not Protective Against Malaria, But is Associated with Anemia in Children Under 5 Years in South Kivu/Democratic Republic of Congo with Malaria. SSRN Electronic Journal.
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