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Renal carnitine transport defect

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Data Correlations | 1 study

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Genes category icon Genes
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SLC22A5 100 100
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Biogroups category icon Biogroups
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Sugar transporter, conserved site 100 100
Major facilitator superfamily MFS-1 100 100
Major facilitator superfamily 99 99
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Individual Studies

  • Mouse Phenotypes - Kidney diseases

    Mus musculus Mus musculus | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated mouse gene mutation data extracted from the Mouse Genome Database (MGD) at The Jackson Laboratory, Bar Harbor, Maine. Additional computational processing and curation of mouse phenotype data was performed to further organize and group data from related phenotypes into uni…

    Source: NextBio Library/Mutation and Phenotypic data
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Associated Researchers

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Thought leaders and organizations working on research involving primary carnitine deficiency.

View All Author iconAuthors
  • N Longo
  • Y Wang
  • Nicola Longo
  • Cristina Amat di San Filippo
  • B Garavaglia
View All Clinical trial sponsors icon Clinical Trials Sponsors
  • University Hospital, Tours
  • Assistance Publique - Hôpitaux de Paris
  • National Center for Complementary and Alternative Medicine (NCCAM)
  • National Institute of Nursing Research (NINR)
  • Rigshospitalet, Denmark
View All Affiliations icon Organizations
  • Emory University
  • University of Utah
  • Chinese University of Hong Kong
  • Akita University School of Medicine
  • University of Minnesota

Clinical Trials | 14 trials

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