Results
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15241.
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15242.
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15246.
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15247.
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15248.
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15249.
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Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function. [electronic resource] by
- Lehnart, Stephan E
- Ackerman, Michael J
- Benson, D Woodrow
- Brugada, Ramon
- Clancy, Colleen E
- Donahue, J Kevin
- George, Alfred L
- Grant, Augustus O
- Groft, Stephen C
- January, Craig T
- Lathrop, David A
- Lederer, W Jonathan
- Makielski, Jonathan C
- Mohler, Peter J
- Moss, Arthur
- Nerbonne, Jeanne M
- Olson, Timothy M
- Przywara, Dennis A
- Towbin, Jeffrey A
- Wang, Lan-Hsiang
- Marks, Andrew R
Producer: 20071218
In:
Circulation vol. 116
Availability: No items available.
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15250.
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15251.
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15252.
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15253.
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15254.
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15255.
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15256.
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15257.
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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. [electronic resource] by
- Arnestad, Marianne
- Crotti, Lia
- Rognum, Torleiv O
- Insolia, Roberto
- Pedrazzini, Matteo
- Ferrandi, Chiara
- Vege, Ashild
- Wang, Dao W
- Rhodes, Troy E
- George, Alfred L
- Schwartz, Peter J
Producer: 20070214
In:
Circulation vol. 115
Availability: No items available.
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15258.
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Cardiac sodium channel dysfunction in sudden infant death syndrome. [electronic resource] by
- Wang, Dao W
- Desai, Reshma R
- Crotti, Lia
- Arnestad, Marianne
- Insolia, Roberto
- Pedrazzini, Matteo
- Ferrandi, Chiara
- Vege, Ashild
- Rognum, Torleiv
- Schwartz, Peter J
- George, Alfred L
Producer: 20070214
In:
Circulation vol. 115
Availability: No items available.
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15259.
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15260.
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