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

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

DOI

https://doi.org/10.1016/j.ajhg.2016.06.025
Final published version

Pasquelena de Nittis
Charlotte D. Koopman
Wojciech Wiszniewski
Carolina Fischinger Moura de Souza
Nicolas Guex
Valerio Napolioni
Federico Tessadori
Lamiae Boualla
Wim de Graaff
Dario Cocciadiferro
Natascia Malerba
Barbara Mandriani
Zeynep Hande Coban Akdemir
Richard J. Fish
Mohammad K. Eldomery
Ilham Ratbi
Teun de Boer
William F. Simonds
Marguerite Neerman-Arbez
V. Reid Sutton
Fernando Kok
James R. Lupski
Alexandre Reymond
Jeroen Bakkers
Giuseppe Merla

Original language	English
Pages (from-to)	704-710
Journal	American journal of human genetics
Volume	99
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2016.06.025
Publication status	Published - 2016

ID: 2963428