Filtry
Projekt
Clinical significance and electrophysiological evaluation of KCNQ1 gene mutation c.926C>T (p.T309I) as a possible long QT syndrome founder mutation (NV16-30571A)
mutation (c.926C>T; p.T309I-Kv7.1) was present in 5 putatively unrelated LQTS families. This project is aimed at verification of the hypothesis that T309I-Kv7.1 mutation in T309I-Kv7.1 families, new mutation carriers will ...
FA - Kardiovaskulární nemoci včetně kardiochirurgie
- 2016 - 2020 •
- 10 413 tis. Kč •
- 10 381 tis. Kč •
- MZ
Řešení projektu: 1. 4. 2016 - 31. 12. 2020
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
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