“Nuestra experiencia en el diagnóstico genético de enfermedades raras mediante secuenciación completa de exoma (WES)”. Francisco Martínez Azorín (Dept. Bioquímica, Instituto de Investigación H12O).
“Papel de FGF-23 en la aritmogénesis ventricular: Una aproximación traslacional”. Alberto Navarro García (Grupo Hipertensión Arterial y Riesgo Cardiovascular, Instituto de Investigación H12O).
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