Three exonic variants in the COL4A5 gene alter RNA splicing in a minigene assay
Abstract Background X‐linked Alport syndrome (XLAS) is an inherited renal disease caused by rare variants of COL4A5 on chromosome Xq22. Many studies have indicated that single nucleotide variants (SNVs) in exons can disrupt normal splicing process of the pre‐mRNA by altering various splicing regulat...
שמור ב:
| Principais autores: | , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Wiley
2024-02-01
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| סדרה: | Molecular Genetics & Genomic Medicine |
| נושאים: | |
| גישה מקוונת: | https://doi.org/10.1002/mgg3.2395 |
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