Cargando…
Mutation spectrum of ATP7B gene in pediatric patients with Wilson disease in Vietnam
BACKGROUND: Wilson disease (WD) is caused by mutations in the copper-transporting P-type adenosine triphosphatase encoded by the ATP7B gene. In this study, we screened and identified the ATP7B mutations among unrelated Vietnamese pediatric patients. METHODS: One-hundred-thirteen pediatric patients w...
| Autores principales: | , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248214/ https://www.ncbi.nlm.nih.gov/pubmed/35782615 http://dx.doi.org/10.1016/j.ymgmr.2022.100861 |