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Results 1 - 3 of 3 for MCC
  1. 3-methylcrotonyl-CoA carboxylase deficiency 
    3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins. People with this disorder have a shortage of ...
    https://medlineplus.gov/...methylcrotonyl-coa-carboxylase-deficiency - Genetics
  2. MCCC1 gene 
    ... an enzyme called 3-methylcrotonoyl-CoA carboxylase or MCC. These alpha subunits join with smaller beta subunits ... is required for the enzyme to function.The MCC enzyme is found in mitochondria, which are the ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
  3. MCCC2 gene 
    ... an enzyme called 3-methylcrotonoyl-CoA carboxylase or MCC. These beta subunits join with larger alpha subunits ... these pairings together form a functioning enzyme.The MCC enzyme is found in mitochondria, which are the ...
    https://medlineplus.gov/genetics/gene/mccc2 - Genetics