Rapid screening of UPB1 gene variations by high resolution melting curve analysis

The present study aimed to analyze gene mutations in patients with β-ureidopropinoase deficiency and establish a rapid detection method for β-ureidopropinoase (UPB1) pathogenic variations by high resolution melting (HRM) analysis. DNA samples with known UPB1 mutations in three patients with β-ureido...

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Detalles Bibliográficos
Autores principales: Xu, Xiaowei, Zheng, Jie, Zou, Qianqian, Wang, Chao, Zhang, Xinjie, Wang, Xuetao, Liu, Yang, Shu, Jianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938451/
https://www.ncbi.nlm.nih.gov/pubmed/33692834
http://dx.doi.org/10.3892/etm.2021.9834

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938451/
https://www.ncbi.nlm.nih.gov/pubmed/33692834
http://dx.doi.org/10.3892/etm.2021.9834

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