Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. [electronic resource]
Producer: 20120531Description: 1225-31 p. digitalISSN:- 1098-1004
- Base Sequence
- Cardiomyopathy, Hypertrophic -- genetics
- DNA Mutational Analysis
- DNA, Mitochondrial -- chemistry
- Exome
- Female
- Humans
- Infant
- Infant, Newborn
- Male
- Mitochondria -- metabolism
- Mitochondrial Diseases -- genetics
- Mitochondrial Proteins -- genetics
- Molecular Sequence Data
- Mutation
- Ribosomal Proteins -- genetics
- Sequence Deletion
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.