Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy. [electronic resource]
Producer: 20131018Description: 238-47 p. digitalISSN:- 1942-3268
- Adolescent
- Adult
- Age of Onset
- Amino Acid Sequence
- Animals
- Base Sequence
- COS Cells
- Cardiomyopathies -- genetics
- Chlorocebus aethiops
- Female
- Heart Defects, Congenital -- genetics
- Homeobox Protein Nkx-2.5
- Homeodomain Proteins -- chemistry
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Myocytes, Cardiac -- metabolism
- Pedigree
- Proteolysis
- Sequence Alignment
- Transcription Factors -- chemistry
- Transcriptional Activation
- Young Adult
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.