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GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
- Authors :
- Medische Fysiologie
Circulatory Health
Genetica Groep Van Haaften
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
Medische Fysiologie
Circulatory Health
Genetica Groep Van Haaften
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
- Publication Year :
- 2016
Details
- Database :
- OAIster
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1395279998
- Document Type :
- Electronic Resource