Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy (Q77363631)
scientific article published on December 18, 2001
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(P31) (Q13442814)
(P304) 3030-3033
(P407) (Q1860)
(P433) 25
(P478) 104
(P577) Saturday, December 1, 2001
Tuesday, December 18, 2001
(P953) https://www.ahajournals.org/doi/pdf/10.1161/hc5001.102111
https://www.ahajournals.org/doi/full/10.1161/hc5001.102111
(P1433) (Q578091)
(P1476) "Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy" (language: en)
"Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy" (language: en)
(P2093) M. H. Gollob
J. J. Seger
T. N. Gollob
T. Tapscott
O. Gonzales
L. Bachinski
R. Roberts
(P2860) (Q69212446)
(Q28201949)
(Q28139827)
(Q22253261)
(Q24291256)
(Q77109332)
(Q24311343)
(Q64786314)
(Q24617464)
(Q74456171)
(Q36689446)
other details
description scientific article published on December 18, 2001

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