A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A

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Oxford University Press

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Mutations in the RPGR gene cause X-linked cone dystrophy

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Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

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Mutations in the MTM1 Gene Implicated in X-Linked Myotubular Myopathy

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doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

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