APA

Lodder E. M., De Nittis P., Koopman C. D., Wiszniewski W., Moura de Souza C. F., Lahrouchi N., Guex N., Napolioni V., Tessadori F., Beekman L., Nannenberg E. A., Boualla L., Blom N. A., de Graaff W., Kamermans M., Cocciadiferro D., Malerba N., Mandriani B., Coban Akdemir Z. H., Fish R. J., Eldomery M. K., Ratbi I., Wilde A. A. M., de Boer T., Simonds W. F., Neerman-Arbez M., Sutton V. R., Kok F., Lupski J. R., Reymond A., Bezzina C. R., Bakkers J. & Merla G. (092016). GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. : American journal of human genetics.

Chicago

Lodder Elisabeth M, De Nittis Pasquelena, Koopman Charlotte D, Wiszniewski Wojciech, Moura de Souza Carolina Fischinger, Lahrouchi Najim, Guex Nicolas, Napolioni Valerio, Tessadori Federico, Beekman Leander, Nannenberg Eline A, Boualla Lamiae, Blom Nico A, de Graaff Wim, Kamermans Maarten, Cocciadiferro Dario, Malerba Natascia, Mandriani Barbara, Coban Akdemir Zeynep Hande, Fish Richard J, Eldomery Mohammad K, Ratbi Ilham, Wilde Arthur A M, de Boer Teun, Simonds William F, Neerman-Arbez Marguerite, Sutton V Reid, Kok Fernando, Lupski James R, Reymond Alexandre, Bezzina Connie R, Bakkers Jeroen and Merla Giuseppe. 092016. GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. : American journal of human genetics.

Harvard

Lodder E. M., De Nittis P., Koopman C. D., Wiszniewski W., Moura de Souza C. F., Lahrouchi N., Guex N., Napolioni V., Tessadori F., Beekman L., Nannenberg E. A., Boualla L., Blom N. A., de Graaff W., Kamermans M., Cocciadiferro D., Malerba N., Mandriani B., Coban Akdemir Z. H., Fish R. J., Eldomery M. K., Ratbi I., Wilde A. A. M., de Boer T., Simonds W. F., Neerman-Arbez M., Sutton V. R., Kok F., Lupski J. R., Reymond A., Bezzina C. R., Bakkers J. and Merla G. (092016). GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. : American journal of human genetics.

MLA

Lodder Elisabeth M, De Nittis Pasquelena, Koopman Charlotte D, Wiszniewski Wojciech, Moura de Souza Carolina Fischinger, Lahrouchi Najim, Guex Nicolas, Napolioni Valerio, Tessadori Federico, Beekman Leander, Nannenberg Eline A, Boualla Lamiae, Blom Nico A, de Graaff Wim, Kamermans Maarten, Cocciadiferro Dario, Malerba Natascia, Mandriani Barbara, Coban Akdemir Zeynep Hande, Fish Richard J, Eldomery Mohammad K, Ratbi Ilham, Wilde Arthur A M, de Boer Teun, Simonds William F, Neerman-Arbez Marguerite, Sutton V Reid, Kok Fernando, Lupski James R, Reymond Alexandre, Bezzina Connie R, Bakkers Jeroen and Merla Giuseppe. GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. : American journal of human genetics. 092016.