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Tyrosinemia, type I

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Individual Studies
  • Mouse Phenotypes - Specific enzyme deficiency

    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

  • OMIM - Congenital disorder

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data

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Thought leaders and organizations working on research involving tyrosinemia type i.

  • P J McKiernan
  • M A Preece
  • M Grompe
  • M Al-Dhalimy
  • M Finegold
  • National Center for Research Resources (NCRR)
  • FDA Office of Orphan Products Development
  • Allergy Therapeutics
  • National Human Genome Research Institute (NHGRI)
  • Birmingham Children's Hospital
  • Université Laval
  • Mayo Clinic College of Medicine
  • University Medical Center
  • University of Istanbul

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