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Clinical exome sequencing is frequently used to identify gene-disrupting variants in individuals with neurodevelopmental disorders. While splice-disrupting variants are known to contribute to these disorders, clinical interpretation of cryptic splice variants outside of the canonical splice site has been challenging. Here, we discuss papers that improve such detection.

Original publication

DOI

10.1186/s13073-020-00737-2

Type

Journal article

Journal

Genome Medicine

Publication Date

24/04/2020

Volume

12