SEMA6A

5q22.3-q23.3 interstitial deletion with neuronal migration defect

1 article(s) in the watch · Constitutional genetics

Curated publications

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

5q22.3-q23.3 interstitial deletion with neuronal migration defect

Gén.1 September 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.