A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome

Lady J Ríos-Serna1 Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Valle del Cauca, Colombia, [email protected]

Lorena Díaz-Ordoñez1 Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Valle del Cauca, Colombia, [email protected]

Estephania Candelo1 Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Valle del Cauca, Colombia, [email protected];2 Biomaterial and Tissues Engineering and Genetic of Human Diseases, University College London, London, UK

Harry Pachajoa1 Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Valle del Cauca, Colombia, [email protected];3 Fundación Valle del Lili, Cali, Valle del Cauca, Colombia, [email protected]Correspondence[email protected]

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A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome

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A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome

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