B. Mutlu Et Al. , "A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy," European Society of Cardiology Congress , Stockholm, Sweden, pp.1270, 2005
Mutlu, B. Et Al. 2005. A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy. European Society of Cardiology Congress , (Stockholm, Sweden), 1270.
Mutlu, B., Bayrak, A. E., Bayrak, F., Kahveci, G., & Ünaltuna, N., (2005). A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy . European Society of Cardiology Congress (pp.1270). Stockholm, Sweden
Mutlu, Bülent Et Al. "A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy," European Society of Cardiology Congress, Stockholm, Sweden, 2005
Mutlu, Bülent Et Al. "A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy." European Society of Cardiology Congress , Stockholm, Sweden, pp.1270, 2005
Mutlu, B. Et Al. (2005) . "A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy." European Society of Cardiology Congress , Stockholm, Sweden, p.1270.
@conferencepaper{conferencepaper, author={Bülent Mutlu Et Al. }, title={A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy}, congress name={European Society of Cardiology Congress}, city={Stockholm}, country={Sweden}, year={2005}, pages={1270} }