Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families. [electronic resource]
Producer: 20170502Description: 83 p. digitalISSN:- 1471-2350
- Amino Acids -- genetics
- Cardiomyopathy, Dilated -- diagnostic imaging
- DNA -- chemistry
- DNA Mutational Analysis
- Death, Sudden, Cardiac -- etiology
- Electrocardiography
- Female
- Genotype
- High-Throughput Nucleotide Sequencing
- Homeobox Protein Nkx-2.5 -- genetics
- Humans
- Male
- Pedigree
- Phenotype
- Polymorphism, Single Nucleotide
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Publication Type: Journal Article
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