A novel mutation in PRKAG2 responsible for familial Wolff-Parkinson-White syndrome and severe cardiac hypertrophy | AVESİS

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A novel mutation in PRKAG2 responsible for familial Wolff-Parkinson-White syndrome and severe cardiac hypertrophy

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MUTLU B., BAYRAK E. K., BAYRAK F., KAHVECI G., BASARAN Y., Unaltuna N.

27th Congress of the European-Society-of-Cardiology, Stockholm, Sweden, 3 - 07 September 2005, vol.26, pp.198

Publication Type: Conference Paper / Summary Text
Volume: 26
City: Stockholm
Country: Sweden
Page Numbers: pp.198
Istanbul University Affiliated: Yes