Bi-allelic variants in TM2D3 cause a severe syndromic neurodevelopmental disorder associated with endoplasmic reticulum and mitochondrial abnormalities
Titel:
Bi-allelic variants in TM2D3 cause a severe syndromic neurodevelopmental disorder associated with endoplasmic reticulum and mitochondrial abnormalities
Auteur:
Gabillard-Lefort, Claudie Martinez, Caroline Silveira Gueguen, Naïg Desquiret-Dumas, Valérie Wery, Méline Legoff, Louis Guimier, Anne Rondeau, Sophie Barcia, Giulia Barnerias, Christine Cogne, Benjamin Besnard, Thomas Lorino, Elsa Douglas, Jessica Bodamer, Olaf Vetro, Annalisa Guerrini, Renzo Balestrini, Simona Conti, Valerio Siri, Laura Chevrollier, Arnaud Bris, Céline Colin, Estelle Procaccio, Vincent Prunier-Mirebeau, Delphine Lenaers, Guy Khiati, Salim Nizon, Mathilde Baris, Olivier R.