ArticleOrphanet journal of rare diseases2026

Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly.

Christiane R Proepper et al.PubMed ↗Full text ↗Publisher ↗

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