Associated Papers
Synonymous and non-synonymous variants at splice junctions can disrupt splicing and are frequently linked to disease associated loss of function genes.
Srinivasan S et al.
Bmc Genomics, 2025
41436921 (PubMed )
Supplement: 12864_2025_12466_MOESM15_ESM.pdf
Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing.
Aoto Y et al.
Kidney International Reports, 2022
Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.
Horinouchi T et al.
Journal of the American Society of Nephrology : Jasn, 2018
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