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QuickView for LINC01551;jsessionid=1F30A844D4C7037914BC83B267E576EC (gene)


Body Atlas

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Disease Atlas

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Pharmaco Atlas

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Knockdown Atlas

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Curated Studies

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Literature

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  1. A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome.
  2. Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and s…
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Clinical Trials

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There were no clinical trials for LINC01551;jsessionid=1F30A844D4C7037914BC83B267E576EC
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