Genomic variants causing abnormal splicing play important roles in genetic disorders and cancer development. Among them, variants that cause the formation of novel splice-sites (splice-site creating ...
Of the ten likely causal variants found in SCLT1, four were missense (c.1631A>G p.(Lys544Arg); c.439G>T p.(Ala147Ser); c.671T>G p.(Leu224Arg); c.1706G>A p.(Ser569Asn)), two were single amino acid ...
Transcribe, splice, and everything’s nice—at least in healthy people. Scientists are finding that abnormal splicing, and genetic variants that cause it, may kickstart some neurodegenerative diseases.
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