3 Matching Annotations
  1. Dec 2024
  2. 52.53.155.43 52.53.155.43
    182235.1-20241125114917-covered-e0fd13ba177f913fd3156f593ead4cfd-html.html
    1
    1. scibot 06 Dec 2024
      RRID:MMRRC_000426-UCD

      DOI: 10.1172/jci182235

      Resource: RRID:MMRRC_000426-UCD

      Curator: @scibot

      SciCrunch record: RRID:MMRRC_000426-UCD

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      RRID:MMRRC_000426-UCD
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    52.53.155.43/a3bf908ac8f053b74109503450248bbf3b51bb8b/182235.1-20241125114917-covered-e0fd13ba177f913fd3156f593ead4cfd-html.html
  3. Oct 2024
  4. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Patient-derived SLC6A1 variant S295L results in an epileptic phenotype similar to haploinsufficient mice
    1
    1. scibot 04 Oct 2024
      RRID:MMRRC_000426-UCD

      DOI: 10.1111/epi.17731

      Resource: RRID:MMRRC_000426-UCD

      Curator: @scibot

      SciCrunch record: RRID:MMRRC_000426-UCD

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      RRID:MMRRC_000426-UCD
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    ncbi.nlm.nih.gov/pmc/articles/PMC10592270/
  5. Mar 2023
  6. www.biorxiv.org www.biorxiv.org
    Electrobehavioral phenotype and seizure pharmacosensitivity in a novel mouse model of patient-derived SLC6A1 S295L mutation-associated neurodevelopmental epilepsy
    1
    1. scibot 21 Mar 2023
      RRID:MMRRC_000426-UCD

      DOI: 10.1101/2021.12.17.473036

      Resource: MMRRC_000426-UCD

      Curator: @scibot

      SciCrunch record: RRID:MMRRC_000426-UCD

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      RRID:MMRRC_000426-UCD
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    biorxiv.org/content/10.1101/2021.12.17.473036v1