Cargando…
Association of genetic variants of the vitamin D receptor gene with vitiligo in a tertiary care center in a Saudi population: a case-control study
BACKGROUND: Vitiligo is a common cutaneous disorder of the skin and hair caused by a systemic depigmentation disorder that affects 1% of the population or less due to its onset in early adulthood. Meta-analyses have documented a linkage between vitiligo and the vitamin D receptor (VDR) gene. OBJECTI...
Autores principales: | Saif, Ghada Bin, Khan, Imran Ali |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982003/ https://www.ncbi.nlm.nih.gov/pubmed/35380061 http://dx.doi.org/10.5144/0256-4947.2022.96 |
Ejemplares similares
-
Evaluation of CAT Variants A-89T, C389T, and C419T in Patients with Vitiligo in the Saudi Population
por: Saif, Ghada A. Bin, et al.
Publicado: (2023) -
Vitamin D Receptor Expression in Vitiligo
por: Doss, Reham William, et al.
Publicado: (2015) -
Relevance of Serum Levels and Functional Genetic Variants in Vitamin D Receptor Gene among Saudi Women with Gestational Diabetes Mellitus
por: Ali Khan, Imran, et al.
Publicado: (2023) -
Association of CYP2C9 Genetic Variants with Vitiligo
por: Alzolibani, Abdullateef A., et al.
Publicado: (2014) -
Association Between Vitamin D, Zinc, and Thyroid Biomarker Levels With Vitiligo Disease: A Retrospective Cohort Study in a Tertiary Care Center
por: Bashrahil, Bader, et al.
Publicado: (2022)