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Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis.

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https://www.hal.inserm.fr/inserm-01074523
Contributor : Mireille Bos <>
Submitted on : Tuesday, October 14, 2014 - 4:29:57 PM
Last modification on : Tuesday, October 14, 2014 - 4:30:00 PM

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  • HAL Id : inserm-01074523, version 1
  • PUBMED : 25305082

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Pierre Billuart. Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis.. Human Molecular Genetics, Oxford University Press (OUP), 2014, pp.ddu523. ⟨inserm-01074523⟩

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