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Results 1 - 6 of 6 for Levocarnitine
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  1. SLC22A5 gene 
    ... membrane, where it transports a substance known as carnitine into the cell. Carnitine is mainly obtained from food and is needed ... SLC22A5 gene have been found to cause primary carnitine deficiency. Some of these variants create a premature ...
    https://medlineplus.gov/genetics/gene/slc22a5 - Genetics
  2. CPT1A gene 
    ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 1A, which is found in the liver. ... first be attached to a substance known as carnitine. Carnitine palmitoyltransferase 1A connects carnitine to long-chain ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  3. CPT2 gene 
    ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 2. This enzyme is essential for fatty ... acids must first attach to a compound called carnitine. Once inside mitochondria, carnitine palmitoyltransferase 2 removes the ...
    https://medlineplus.gov/genetics/gene/cpt2 - Genetics
  4. SLC25A20 gene 
    ... gene provides instructions for making a protein called carnitine-acylcarnitine translocase (CACT). This protein is essential for ... must be attached to a substance known as carnitine to enter mitochondria. Once these fatty acids are ...
    https://medlineplus.gov/genetics/gene/slc25a20 - Genetics
  5. ACAD8 gene 
    ... disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. Pediatr ... in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening. Pediatr ...
    https://medlineplus.gov/genetics/gene/acad8 - Genetics
  6. ACADS gene 
    ... is common but not associated with increased C4-carnitine in newborn blood spots. J Inherit Metab Dis. ...
    https://medlineplus.gov/genetics/gene/acads - Genetics