Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder-Reference-Cited by-同舟云学术

Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder

Published:2023-11 Issue:11 Volume:25 Page:100922
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Pavinato Lisa,Stanic Jennifer,Barzasi Marta,Gurgone Antonia,Chiantia Giuseppe,Cipriani Valentina,Eberini Ivano,Palazzolo Luca,Di Luca Monica,Costa Alex,Marcantoni Andrea,Biamino Elisa,Spada Marco,Hiatt Susan M.,Kelley Whitley V.,Vestito Letizia,Sisodiya Sanjay M.,Efthymiou Stephanie,Chand Prem,Kaiyrzhanov Rauan,Bruselles Alessandro,Cardaropoli Simona,Tartaglia Marco,De Rubeis Silvia,Buxbaum Joseph D.,Smedley Damian,Ferrero Giovanni Battista,Giustetto Maurizio,Gardoni Fabrizio,Brusco Alfredo

Publisher

Elsevier BV

Subject

Genetics (clinical)

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