A Novel Intronic Variant in FRMPD4 Disrupts Splicing: Case Report of an X-Linked Neurodevelopmental Disorder

Tomoko Satake1,2, Yasuhiro Kawai1, Koki Nagai1

  • 1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.

Summary

A novel genetic variant in the FRMPD4 gene was identified in a boy with developmental delay. This intronic variant disrupts splicing, potentially causing neurodevelopmental disorder by affecting a key neuronal protein.

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