GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability

Elisabeth M M. Lodder, Pasquelena De Nittis, Charlotte D D. Koopman, Wojciech Wiszniewski, Carolina Fischinger F. Moura de Souza, Najim Lahrouchi, Nicolas Guex, Valerio Napolioni, Federico Tessadori, Leander Beekman, Eline A A. Nannenberg, Lamiae Boualla, Nico A A. Blom, Wim de Graaff, Maarten Kamermans, Dario Cocciadiferro, Natascia Malerba, Barbara Mandriani, Zeynep Hande Coban H.C. Akdemir, Richard J J. FishMohammad K K. Eldomery, Ilham Ratbi, Arthur A A.M. Wilde, Teun de Boer, William F F. Simonds, Marguerite Neerman-Arbez, V. Reid Sutton, Fernando Kok, James R R. Lupski, Alexandre Reymond, Connie R R. Bezzina, Jeroen Bakkers, Giuseppe Merla

Research output: Contribution to journal › Article › peer-review

46 Scopus citations

Fingerprint

Dive into the research topics of 'GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability'. Together they form a unique fingerprint.

Medicine & Life Sciences