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Author

Lisa Forman

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Case report Sep 2026

Expansion of the Clinical and Molecular Spectrum of LINS1-Associated Disease.

LINS1 gene plays a role in cognition and brain development. Mutations in this gene have been identified as the cause of a neurodevelopmental disorder as well as dysmorphisms, motor symptoms, behavioral problems, seizures, microcephaly, mitral valve prolapse, and Q-T prolongation. We recruited two related families with...

A. Ibrahim, Erik Levine, Ayuko Iverson et al. · 0 citations

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