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Deficiency of methylcrotonoyl-CoA carboxylase

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Data Correlations | 1 study

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Genes category icon Genes
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MCCC1 100 100
MCCC2 100 100
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Biogroups category icon Biogroups
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Valine Leucine and Isoleucine Degra… 100 100
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Individual Studies

  • 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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Associated Researchers

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Thought leaders and organizations working on research involving 3-methylcrotonyl coa carboxylase deficiency.

View All Author iconAuthors
  • T Suormala
  • E R Baumgartner
  • Matthias R Baumgartner
  • M R Baumgartner
  • Terttu Suormala
View All Affiliations icon Organizations
  • University Children's Hospital
  • Ludwig-Maximilians-University
  • Duke University Medical Center
  • Shanghai Jiao Tong University School of Medicine
  • University Hospitals Case Medical Center

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