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GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. [electronic resource] by
- 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
- Akdemir, Zeynep Hande Coban
- 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
- Merla, Giuseppe
Producer: 20170502
In:
American journal of human genetics vol. 99
Availability: No items available.
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