Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children. [electronic resource]
Producer: 20020213Description: 177-81 p. digitalISSN:- 0022-0736
- Adolescent
- Adult
- Cation Transport Proteins
- Child
- Child, Preschool
- DNA-Binding Proteins
- Death, Sudden, Cardiac -- etiology
- ERG1 Potassium Channel
- Ether-A-Go-Go Potassium Channels
- Humans
- Infant
- KCNQ Potassium Channels
- KCNQ1 Potassium Channel
- Long QT Syndrome -- genetics
- Mutation
- NAV1.5 Voltage-Gated Sodium Channel
- Potassium Channels -- genetics
- Potassium Channels, Voltage-Gated
- Sodium Channels -- genetics
- Sudden Infant Death -- genetics
- Trans-Activators
- Transcriptional Regulator ERG
- Ventricular Fibrillation -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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