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3. Ont collaboré à cet ouvrage

5. Editorial

7. Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction Disease

8. Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome

9. Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction Disease.

10. Gain-of-Function Mutations in TRPM4Cause Autosomal Dominant Isolated Cardiac Conduction Disease

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