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ArticleEuropean journal of human genetics : EJHG2025

CASP2 biallelic truncating variants: a new case supports the link with lissencephaly/pachygyria and expands the clinical spectrum.

Ilaria Vivaldi et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 39672921