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BCLAF3

HGNC ↗

X-linked neurodevelopmental disorder

1 article(s) in the watch · Constitutional genetics

Curated publications

10/10

Multiomic approaches identify a rare CCG repeat expansion in BCLAF3 in neurodevelopmental disorders.

X-linked neurodevelopmental disorder

Gén.28 July 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.