Cargando…
Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients
BACKGROUND: Hemoglobinopathies, inherited disorders of hemoglobin (Hb), are the most common hereditary monogenic diseases of the red cell in the world. Few studies have been conducted on hemoglobinopathies in Mauritania. Therefore, the aim of this work is to establish the molecular and epidemiologic...
Autores principales: | Mahmoud, Taher, Sahli, Chaima, Hadj Fredj, Sondess, Amri, Yessine, Othmani, Rim, Mohamed, Ghaber S., Zein, Ekhtelbenina, Messaoud, Taieb |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544207/ https://www.ncbi.nlm.nih.gov/pubmed/36106931 http://dx.doi.org/10.1002/mgg3.2048 |
Ejemplares similares
-
Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
por: Chkioua, Latifa, et al.
Publicado: (2021) -
Osteoporosis-Pseudoglioma in a Mauritanian Child due to a Novel Mutation in LRP5
por: Biha, Noura, et al.
Publicado: (2016) -
Screening of BRCA1/2 variants in Mauritanian breast cancer patients
por: Brahim, Selma Mohamed, et al.
Publicado: (2022) -
HLA class I (-A, -B, -C) and class II (-DR, -DQ) polymorphism in the Mauritanian population
por: Hamed, Cheikh Tijani, et al.
Publicado: (2018) -
Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b
por: Chkioua, Latifa, et al.
Publicado: (2023)