학술논문

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
Document Type
Short Communication
Author
Hannah, Michael G.Bugiardini, EnricoBertini, EnricoKriouile, YamnaEl-Khorassani, MohamedAguennouz, MhammedGroppa, StanislavKarashova, Blagovesta M.Goraya, Jatinder S.Sultan, TipuAvdjieva, DanielaKathom, HadilTincheva, RadkaBanu, SelinaVeggiotti, PierangeloVerrotti, AlbertoLanari, MarcelloSavasta, SalvatoreMacaya, AlfonsGaravaglia, BarbaraBorgione, EugeniaPapacostas, SavvasVikelis, MichailChelban, VioricaKaiyrzhanov, RauanCortese, AndreaSullivan, RoisinPapanicolaou, Eleni Z.Dardiotis, EfthymiosMaqbool, ShaziaIbrahim, ShahnazKirmani, SalmanRana, Nuzhat N.Atawneh, OsamaLim, Shen-YangZuccotti, Gian V.Marseglia, Gian L.Esposito, SusannaShaikh, FarooqCogo, PaolaCorsello, GiovanniMangano, SalvatoreNardello, RosariaMangano, DonatoScardamaglia, AnnaritaKoutsis, GeorgeScuderi, CarmelaFerrara, PietroMorello, GiovannaZollo, MassimoBerni-Canani, RobertoTerracciano, Luigi M.Sisto, AntonioDi Fabio, SandraStrano, FedericaScorrano, GiovannaDi Bella, SaverioDi Francesco, LudovicaManizha, GanievaIsrofilov, MaksudGuliyeva, UlviyyaSalayev, KamranKhachatryan, SamsonXiromerisiou, GeorgiaSpanaki, CleantheFiorillo, ChiaraIacomino, MicheleGaudio, EugenioMunell, FrancinaGagliano, AntonellaJan, FaridaChimenz, RobertoGitto, EloisaIughetti, LorenzoDi Rosa, GabriellaMaghnie, MohamadPettoello-Mantovani, MassimoGupta, NeerjaKabra, MadhulikaBenrhouma, HaneneTazir, MeriemBottone, GabriellaFarello, GiovanniDelvecchio, MaurizioDi-Donato, GiulioObeid, MakramBakhtadze, SophiaSaadi, Nebal W.Miraglia-Del-Giudice, MicheleMaccarone, RitaZaki, Maha S.Triki, Chahnez C.Kara, MajdiKarimiani, Ehsan G.Salih, Ahmed M.Ramenghi, Luca A.Seri, MarcoDi-Falco, GiovannaMandarà, LuanaBarrano, GiuseppeElisa, MaurizioCherubini, EnricoOperto, Francesca F.Valenzise, MariellaCattaneo, AntoninoZazzeroni, FrancescaAlesse, EdoardoMatricardi, SaraZafar, FaisalUllah, EhsanAfzal, ErumRahman, FatimaAhmed, Muhammad M.Parisi, PasqualeSpalice, AlbertoDe Filippo, MariaLicari, AmeliaTrebbi, EdoardoRomano, FerdinandoHeimer, GaliAl-Khawaja, IssamAl-Mutairi, FuadAlkuraya, Fowzan S.Rizig, MieShashkin, ChingizZharkynbekova, NaziraKoneyev, KairgaliSalpietro, VincenzoMaroofian, RezaWangen, JamieCiolfi, AndreaBarresi, SabinaEfthymiou, StephanieLamaze, AngeliqueAughey, Gabriel N.Al Mutairi, FuadRad, AboulfazlRocca, ClarissaCalì, ElisaAccogli, AndreaZara, FedericoStriano, PasqualeMojarrad, MajidTariq, HumaGiacopuzzi, EdoardoTaylor, Jenny C.Oprea, GabrielaSkrahina, VolhaRehman, Khalil UrAbd Elmaksoud, MarwaBassiony, MahmoudEl Said, Huda G.Abdel-Hamid, Mohamed S.Al Shalan, MahaSeo, GohunKim, SohyunLee, HaneKhang, RinIssa, Mahmoud Y.Elbendary, Hasnaa M.Rafat, KarimaMarinakis, Nikolaos M.Traeger-Synodinos, JoanneVerveri, AthinaSourmpi, MaraEslahi, AtiehKhadivi Zand, FarhadBeiraghi Toosi, MehranBabaei, MeisamJackson, AdamBertoli-Avella, AidaPagnamenta, Alistair T.Niceta, MarcelloBattini, RobertaCorsello, AntonioLeoni, ChiaraChiarelli, FrancescoDallapiccola, BrunoFaqeih, Eissa AliTallur, Krishnaraya K.Alfadhel, MajidAlobeid, EmanMaddirevula, SateeshMankad, KshitijBanka, SiddharthGhayoor-Karimiani, EhsanTartaglia, MarcoChung, Wendy K.Green, RachelJepson, James E.C.Houlden, Henry
Source
In The American Journal of Human Genetics 4 January 2024 111(1):200-210
Subject
Language
ISSN
0002-9297