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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 4
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Original Article

Hb S [β6(A3)Glu→Val, GAG>GTG] and β-Globin Gene Cluster Haplotype Distribution in Mauritania

Fatimetou M. VetenDépartment de Biologie, Faculté des Sciences et Techniques, Nouakchott, Mauritanie
,
Isselmou O. AbdelhamidDépartment de Biochimie et Hématologie, Centre Hospitalier National, Nouakchott, Mauritanie
,
Ghlana M. MeiloudDépartment de Biologie, Faculté des Sciences et Techniques, Nouakchott, Mauritanie
,
Sidi M GhaberDépartment de Biochimie et Hématologie, Centre Hospitalier National, Nouakchott, Mauritanie
,
Mohamed L. SalemDépartment de Biochimie et Hématologie, Centre Hospitalier National, Nouakchott, Mauritanie
,
Salem AbbesLaboratoire d’Hématologie Moléculaire et Cellulaire, Institut Pasteur de Tunis, Tunis, Tunisie
&
Ahmed O. HoumeidaDépartment de Biologie, Faculté des Sciences et Techniques, Nouakchott, MauritanieCorrespondence[email protected]
 show all
Pages 311-315 | Received 26 Sep 2011, Accepted 28 Feb 2012, Published online: 24 May 2012

Citations (10)

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Fatimetou Veten, Sidi Ghaber, Nordine Habti & Ahmed Houmeida. (2015) Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population. Hemoglobin 39:4, pages 296-297.
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Articles from other publishers (9)

Kevin K Esoh, Tobias O Apinjoh, Alfred Amambua-Ngwa, Steven G Nyanjom, Emile R Chimusa, Lucas Amenga-Etego, Ambroise Wonkam & Eric A Achidi. (2023) Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. Human Molecular Genetics 32:12, pages 1946-1958.
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Taher Mahmoud, Chaima Sahli, Sondess Hadj Fredj, Yessine Amri, Rim Othmani, Ghaber S. Mohamed, Ekhtelbenina Zein & Taieb Messaoud. (2022) Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients. Molecular Genetics & Genomic Medicine 10:10.
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NoorTaha Yaseen, HindShaker Al-Mamoori & Mea`adKadhum Hassan. (2020) Sickle ß-globin haplotypes among patients with sickle cell anemia in Basra, Iraq: A cross-sectional study. Iraqi Journal of Hematology 9:1, pages 23.
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Lilia Romdhane, Olfa Messaoud, Rym Kefi, Afaf Tiar, Ahlem Amouri, Mourad Mokni, Neji Tebib, Mohamed Zghal, Abdelhamid Barakat, Ahmed Houmeida, Mariem Bozguiya, Mohamed Othman, Ghada El-Kamah & Sonia Abdelhak. 2019. The Genetics of African Populations in Health and Disease. The Genetics of African Populations in Health and Disease 233 267 .
Ely Cheikh Mohamed Moctar, Zied Riahi, Hala El Hachmi, Fatimetou Veten, Ghlana Meiloud, Christine Bonnet, Sonia Abdelhak, Mohammed Errami & Ahmed Houmeida. (2016) Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss. European Archives of Oto-Rhino-Laryngology 273:11, pages 3693-3698.
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Juliana D. Lindenau, Sandrine C. Wagner, Simone M. de Castro & Mara H. Hutz. (2016) The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes. Genetics and Molecular Biology 39:4, pages 515-523.
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Valentina J. Ngo BitounguiGift D. PuleNeil HanchardJeanne NgogangAmbroise Wonkam. (2015) Beta-Globin Gene Haplotypes Among Cameroonians and Review of the Global Distribution: Is There a Case for a Single Sickle Mutation Origin in Africa?. OMICS: A Journal of Integrative Biology 19:3, pages 171-179.
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Isselmou Abdelhamid, Khaled Lasram, Ghlana Meiloud, Nizar Ben Halim, Rym Kefi, Abdoulaye Samb, Sonia Abdelhak & Ahmed Houmeida. (2014) E23K variant in KCNJ11 gene is associated with susceptibility to type 2 diabetes in the Mauritanian population. Primary Care Diabetes 8:2, pages 171-175.
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Khaled Lasram, Nizar Ben Halim, Sana Hsouna, Rym Kefi, Imen Arfa, Welid Ghazouani, Henda Jamoussi, Houda Benrahma, Najla Kharrat, Ahmed Rebai, Slim Ben Ammar, Sonia Bahri, Abdelhamid Barakat, Abdelmajid Abid & Sonia Abdelhak. (2014) Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis . BioMed Research International 2014, pages 1-9.
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