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Open Access

Peer-reviewed

Research Article

Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana

Narcisse Elenga ,

Roles Conceptualization, Data curation, Formal analysis, Methodology, Supervision, Validation, Writing – original draft

* E-mail: elengafr@yahoo.fr

Affiliation Pediatric Unit, Cayenne General Hospital, Cayenne, French Guiana

http://orcid.org/0000-0003-0624-4180

⨯
Emma Cuadro-Alvarez,

Roles Data curation, Writing – review & editing

Affiliation Pediatric Unit, Cayenne General Hospital, Cayenne, French Guiana
⨯
Elise Martin,

Roles Data curation, Writing – review & editing

Affiliation Pediatric Unit, Cayenne General Hospital, Cayenne, French Guiana
⨯
Falucar Njuieyon,

Roles Data curation, Writing – review & editing

Affiliation Pediatric Unit, Cayenne General Hospital, Cayenne, French Guiana
⨯
Antoine Defo,

Roles Data curation, Writing – review & editing

Affiliation Pediatric Unit, Cayenne General Hospital, Cayenne, French Guiana
⨯
Chimène Maniassom

Roles Data curation, Writing – review & editing

Affiliation Pediatric Unit, Cayenne General Hospital, Cayenne, French Guiana
⨯

Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana

Narcisse Elenga,
Emma Cuadro-Alvarez,
Elise Martin,
Falucar Njuieyon,
Antoine Defo,
Chimène Maniassom

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Published: September 3, 2020
https://doi.org/10.1371/journal.pone.0238691

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Haplotypes
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Alpha-thalassemia
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Hemoglobin
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Deletion mutation
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Hematology
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French people
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Mutation
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Sickle cell disease
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