Cargando…
Alpha thalassemia genotypes in Kuwait
BACKGROUND: The frequency of the alpha thalassemia trait is approximately 40% in the Kuwaiti population, but there has been no comprehensive study of the prevalent alleles. This is a report of patients who were referred for molecular diagnosis over a 20-year period. METHODS: This is a retrospective...
Autores principales: | Adekile, Adekunle, Sukumaran, Jalaja, Thomas, Diana, D’Souza, Thomas, Haider, Mohammad |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444039/ https://www.ncbi.nlm.nih.gov/pubmed/32831051 http://dx.doi.org/10.1186/s12881-020-01105-y |
Ejemplares similares
-
Diagnosis of Sickle Cell Disease and HBB Haplotyping in the Era of Personalized Medicine: Role of Next Generation Sequencing
por: Adekile, Adekunle, et al.
Publicado: (2021) -
Unique Polymorphisms at BCL11A, HBS1L-MYB and HBB Loci Associated with HbF in Kuwaiti Patients with Sickle Cell Disease
por: Akbulut-Jeradi, Nagihan, et al.
Publicado: (2021) -
High prevalence of protein tyrosine phosphatase non-receptor N22 gene functional variant R620W in systemic lupus erythematosus patients from Kuwait: implications for disease susceptibility
por: Al-Awadhi, Adel M., et al.
Publicado: (2018) -
Moyamoya syndrome in a child with HbEβ‐thalassemia
por: Zahra, Akmal, et al.
Publicado: (2022) -
Impact of genotype on endocrinal complications of Children with Alpha-thalassemia in China
por: Luo, Hong-Cheng, et al.
Publicado: (2017)