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AMPA receptor GluA2 subunit defects are a cause of neurodev..:
Salpietro, Vincenzo
;
Dixon, Christine L
;
Guo, Hui
...
European Commission 305121. , 2019
Link:
https://ddd.uab.cat/record/224184
RT Journal T1
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
UL https://suche.suub.uni-bremen.de/peid=base-ftuabarcelonapb:oai:ddd.uab.cat:224184&Exemplar=1&LAN=DE A1 Salpietro, Vincenzo A1 Dixon, Christine L A1 Guo, Hui A1 Bello, Oscar D A1 Vandrovcova, Jana A1 Efthymiou, Stephanie A1 Maroofian, Reza A1 Heimer, Gali A1 Burglen, Lydie A1 Valence, Stephanie A1 Torti, Erin A1 Hacke, Moritz A1 Rankin, Julia A1 Tariq, Huma A1 Colin, Estelle A1 Procaccio, Vincent A1 Striano, Pasquale A1 Mankad, Kshitij A1 Lieb, Andreas A1 Chen, Sharon A1 Pisani, Laura A1 Bettencourt, Conceição A1 Männikkö, Roope A1 Manole, Andreea A1 Brusco, Alfredo A1 Grosso, Enrico A1 Ferrero, Giovanni Battista A1 Armstrong, Judith A1 Gueden, Sophie A1 Bar-Yosef, Omer A1 Tzadok, Michal A1 Monaghan, Kristin G A1 Santiago-Sim, Teresa A1 Person, Richard E A1 Cho, Megan T A1 Willaert, Rebecca A1 Yoo, Kristin A1 Chae, Jong-Hee A1 Quan, Yingting A1 Wu, Huidan A1 Wang, Tianyun A1 Bernier, Raphael A A1 Xia, Kun A1 Blesson, Alyssa A1 Jain, Mahim A1 Motazacker, Mohammad M A1 Jaeger, Bregje A1 Schneider, Amy L A1 Boysen, Katja A1 Muir, Alison M A1 Myers, Candance T A1 Gavrilova, Ralitza H A1 Gunderson, Lauren A1 Schultz-Rogers, Laura A1 Klee, Eric W A1 Dyment, David A1 Osmond, Matthew A1 Parellada, Mara A1 Llorente, Cloe A1 González-Peñas, Javier A1 Carracedo, Ángel A1 Van Haeringen, Arie A1 Ruivenkamp, Claudia A1 Nava, Caroline A1 Heron, Delphine A1 Nardello, Rosaria A1 Iacomino, Michele A1 Minetti, Carlo A1 Skabar, Aldo A1 Fabretto, Antonella A1 Hanna, Michael A1 Bugiardini, Enrico A1 Hostettler, Isabel Charlotte A1 O'Callaghan, Benjamin A1 Khan, Alaa A1 Cortese, Andrea A1 O'Connor, Emer A1 Yau, Wai Y A1 Bourinaris, Thomas A1 Kaiyrzhanov, Rauan A1 Chelban, Viorica A1 Madej, Monika A1 Diana, Maria C A1 Vari, Maria S A1 Pedemonte, Marina A1 Bruno, Claudio A1 Balagura, Ganna A1 Scala, Marcello A1 Fiorillo, Chiara A1 Nobili, Lino A1 Malintan, Nancy T A1 Zanetti, Maria N A1 Krishnakumar, Shyam S A1 Lignani, Gabriele A1 Jepson, James E. C A1 Broda, Paolo A1 Baldassari, Simona A1 Rossi, Pia A1 Fruscione, Floriana A1 Madia, Francesca A1 Traverso, Monica A1 De-Marco, Patrizia A1 Pérez-Dueñas, Belén A1 Munell Casadesus, Francina A1 Kriouile, Yamna A1 El-Khorassani, Mohamed A1 Karashova, Blagovesta A1 Avdjieva, Daniela A1 Kathom, Hadil A1 Tincheva, Radka A1 Van-Maldergem, Lionel A1 Nachbauer, Wolfgang A1 Boesch, Sylvia A1 Gagliano, Antonella A1 Amadori, Elisabetta A1 Goraya, Jatinder S A1 Sultan, Tipu A1 Kirmani, Salman A1 Ibrahim, Shahnaz A1 Jan, Farida A1 Mine, Jun A1 Banu, Selina A1 Veggiotti, Pierangelo A1 Zuccotti, Gian V A1 Ferrari, Michel D A1 Van Den Maagdenberg, Arn M. J A1 Verrotti, Alberto A1 Marseglia, Gian Luigi A1 Savasta, Salvatore A1 Soler, Miguel A A1 Scuderi, Carmela A1 Borgione, Eugenia A1 Chimenz, Roberto A1 Gitto, Eloisa A1 Dipasquale, Valeria A1 Sallemi, Alessia A1 Fusco, Monica A1 Cuppari, Caterina A1 Cutrupi, Maria C A1 Ruggieri, Martino A1 Cama, Armando A1 Capra, Valeria A1 Mencacci, Niccolò Emanuele A1 Boles, Richard A1 Gupta, Neerja A1 Kabra, Madhulika A1 Papacostas, Savvas A1 Zamba-Papanicolaou, Eleni A1 Dardiotis, Efthimios A1 Maqbool, Shazia A1 Rana, Nuzhat A1 Atawneh, Osama A1 Lim, Shen Y A1 Shaikh, Mohmad Farooq A1 Koutsis, George A1 Breza, Marianthi A1 Coviello, Domenico A1 Dauvilliers, Yves A1 AlKhawaja, Issam A1 AlKhawaja, Mariam A1 Al-Mutairi, Fuad A1 Stojkovic, Tanya A1 Ferrucci, Veronica A1 Zollo, Massimo A1 Alkuraya, Fowzan S A1 Kinali, Maria A1 Sherifa, Hamed A1 Benrhouma, Hanene A1 Turki, Ilhem B. Y A1 Tazir, Meriem A1 Obeid, Makram A1 Bakhtadze, Sophia A1 Saadi, Marianthi W A1 Zaki, Maha A1 Triki, Chahnez C A1 Benfenati, Fabio A1 Gustincich, Stefano A1 Kara, Majdi A1 Belcastro, Vincenzo A1 Specchio, Nicola A1 Capovilla, Giuseppe A1 Karimiani, Ehsan G A1 Salih, Ahmed M A1 Okubadejo, Njideka A1 Ojo, Oluwadamilola A1 Oshinaike, Olajumoke O A1 Oguntunde, Olapeju A1 Wahab, Kolawole Wasiu A1 Bello, Abiodun H A1 Abubakar, Sanni A1 Obiabo, Yahaya A1 Nwazor, Ernest A1 Ekenze, Oluchi A1 Williams, Uduak A1 Iyagba, Alagoma A1 Taiwo, Lolade A1 Komolafe, Morenikeji A1 Senkevich, Konstantin A1 Shashkin, Chingiz A1 Zharkynbekova, Nazira YR 2019 K1 Next-generation sequencing K1 Synaptic development K1 Ion channels in the nervous system K1 Neurodevelopmental disorders K1 Adolescent K1 Adult K1 Brain K1 Child K1 Preschool K1 Cohort Studies K1 Female K1 Heterozygote K1 Humans K1 Infant K1 Intellectual Disability K1 Loss of Function Mutation K1 Magnetic Resonance Imaging K1 Male K1 Receptors K1 AMPA K1 Young Adult JF European Commission 305121 LK http://dx.doi.org/https://ddd.uab.cat/record/224184 DO https://ddd.uab.cat/record/224184 SF ELIB - SuUB Bremen
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