Hasil Pencarian - Gabriel Cáceres
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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect oleh Christian Veltmann, Hector Barajas‐Martinez, Christian Wolpert, Martin Borggrefe, Rainer Schimpf, Ryan Pfeiffer, Gabriel Cáceres, Elena Burashnikov, Charles Antzelevitch, Dan Hu
Diterbitkan 2016-07-01
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Identification of a novel de novo mutation associated with PRKAG2 cardiac syndrome and early onset of heart failure. oleh Yang Liu, Rong Bai, Lin Wang, Cuntai Zhang, Ruifu Zhao, Deli Wan, Xinshan Chen, Gabriel Caceres, Daniel Barr, Hector Barajas-Martinez, Charles Antzelevitch, Charles Antzelevitch, Dan Hu
Diterbitkan 2013-01-01
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