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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.
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.
Area of Science:
- Genetics
- Neuroscience
- Molecular Biology
Background:
- FRMPD4, located on the X-chromosome, encodes a neuronal scaffold protein implicated in neurodevelopmental disorders.
- Six variants in FRMPD4 have previously been linked to X-linked neurodevelopmental disorder.
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