HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. [electronic resource]
Producer: 20141021Description: 745-56 p. digitalISSN:- 1558-3597
- Adolescent
- Adult
- Aged
- Animals
- CHO Cells
- Cricetulus
- DNA Mutational Analysis
- Exome
- Female
- Genetic Linkage
- Heart Defects, Congenital -- diagnostic imaging
- Humans
- Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels -- genetics
- Male
- Membrane Potentials
- Middle Aged
- Muscle Proteins -- genetics
- Potassium Channels -- genetics
- Sick Sinus Syndrome -- congenital
- Syndrome
- Ultrasonography
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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