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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Exp Ther Med
Päätekijät: Xu, Xiaowei, Zheng, Jie, Zou, Qianqian, Wang, Chao, Zhang, Xinjie, Wang, Xuetao, Liu, Yang, Shu, Jianbo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: D.A. Spandidos 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7938451/
https://ncbi.nlm.nih.gov/pubmed/33692834
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2021.9834
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