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Longer titles found: Carnitine-acylcarnitine translocase deficiency (view)

searching for Carnitine-acylcarnitine translocase 5 found (22 total)

alternate case: carnitine-acylcarnitine translocase

List of disorders included in newborn screening programs (716 words) [view diff] no match in snippet view article find links to article

type 2 Short-chain acyl-CoA dehydrogenase deficiency (SCAD) Carnitine/acylcarnitine Translocase Deficiency (Translocase) Short-chain hydroxy Acyl-CoA dehydrogenase

Β-Hydroxy β-methylbutyryl-CoA (679 words) [view diff] exact match in snippet view article find links to article

membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine translocase (39). 3HIA-carnitine is thought to be either directly deacylated

Β-Hydroxybutyric acid (1,416 words) [view diff] exact match in snippet view article find links to article

membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine translocase (39). 3HIA-carnitine is thought to be either directly deacylated

Leucine (4,132 words) [view diff] exact match in snippet view article find links to article

membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine translocase (39). 3HIA-carnitine is thought to be either directly deacylated

Β-Hydroxy β-methylbutyric acid (9,983 words) [view diff] exact match in snippet view article find links to article

membrane (and hence effectively out of the mitochondria) via carnitine-acylcarnitine translocase (39). 3HIA-carnitine is thought to be either directly deacylated