TTC37 | bioCADDIE Data Discovery Index
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Displaying 2 of 2 results for "TTC37"
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  1. TTC37_XENLA UniProt:Swiss-Prot

    ID: Q6DFB8

    Description: Tetratricopeptide repeat protein 37 TPR 1 TPR 2 TPR 3 TPR 4 TPR 5 TPR 6 TPR 7 TPR 8 TPR 9 TPR 10 TPR 11 TPR 12 TPR 13 TPR 14 TPR 15 TPR 16 TPR 17 TPR ...

    gene.name: ttc37
  2. Consanguinity and Rare Mutations Outside of MCCC Genes Underlie Non-Specific Phenotypes of MCC Deficiency dbGaP

    ID: phs000776.v1.p1

    Description: 3-Methylcrotonyl-CoA Carboxylase Deficiency (MCCD) is an autosomal recessive disorder of leucine catabolism, which has a highly variable clinical phen...

    Study Types: Case-Control

    disease.name: TTC37 protein, human

Displaying 2 of 2 results for "TTC37"