long chain fatty acids

microsomal triglyceride transfer protein ; Homo sapiens







3 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
1 24664533 Mutations in HADHB, which encodes the β-subunit of mitochondrial trifunctional protein, cause infantile onset hypoparathyroidism and peripheral polyneuropathy. 2014 May 2
2 22447425 [Ocular signs of a mitochondrial trifunctional protein defect. A long-term follow-up]. 2012 Mar 1
3 15533621 Maternal heterozygosity for a mitochondrial trifunctional protein mutation as a cause for liver disease in pregnancy. 2005 2