Title : Maternal heterozygosity for a mitochondrial trifunctional protein mutation as a cause for liver disease in pregnancy.

Pub. Date : 2005

PMID : 15533621






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 LCHAD activity resides in the alpha-subunit of the mitochondrial trifunctional protein (MTP), a complex protein that catalyzes beta-oxidation of long chain fatty acids. long chain fatty acids microsomal triglyceride transfer protein Homo sapiens
2 LCHAD activity resides in the alpha-subunit of the mitochondrial trifunctional protein (MTP), a complex protein that catalyzes beta-oxidation of long chain fatty acids. long chain fatty acids microsomal triglyceride transfer protein Homo sapiens