Kirstine Callø
Associate Professor - Promotion Programme
Pathobiological Sciences
Grønnegårdsvej 7
1870 Frederiksberg C
1 - 1 out of 1Page size: 50
- 2010
- Published
A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death
Nof, E., Cordeiro, J. M., Pérez, G. J., Scornik, F. S., Callø, Kirstine, Love, B., Burashnikov, E., Caceres, G., Gunsburg, M. & Antzelevitch, C., 2010, In: Circulation. Cardiovascular genetics. 3, 2, p. 199-206 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5330
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Dysfunction of the heteromeric KV7.3/KV7.5 potassium channel is associated with autism spectrum disorders
Research output: Contribution to journal › Journal article › Research › peer-review
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1495
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Characterization and mechanisms of action of novel NaV1.5 channel mutations associated with Brugada syndrome
Research output: Contribution to journal › Journal article › Research › peer-review
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1433
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Tissue-specific effects of acetylcholine in the canine heart
Research output: Contribution to journal › Journal article › Research › peer-review
Published