Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy. [electronic resource]
Producer: 20030221Description: 101-14 p. digitalISSN:- 0002-9297
- Age of Onset
- Amino Acid Sequence
- Animals
- Base Sequence
- Cardiomyopathy, Hypertrophic -- enzymology
- DNA Mutational Analysis
- Fibroblasts
- Heme -- analogs & derivatives
- Humans
- Membrane Proteins -- biosynthesis
- Mitochondria, Heart -- enzymology
- Molecular Sequence Data
- Mutation -- genetics
- Myocardium -- enzymology
- Saccharomyces cerevisiae Proteins
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.