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Autosomal recessive lissencephaly with cerebellar hypoplasia (LCH) is associated with human reelin gene mutations

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Reelin binds a3&Mac254;1 integrin and inhibits neuronal migration

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DCAMKL1 encodes a protein kinase with homology to Doublecortin that regulates microtubule polymerization in a kinase-independent fashion

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Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation