Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11.2 deletion

Reciprocal Copy Number Variants (CNVs) at the 16p11.2 locus confer high risk for autism spectrum disorder (ASD) and other neurodevelopmental disorders (NDDs). Morphometric MRI studies have revealed large and pervasive volumetric alterations in carriers of a 16p11.2 deletion. However, the specific ne...

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Vydané v:	Translational psychiatry Ročník 14; číslo 1; s. 95 - 11
Hlavní autori:	Maillard, Anne M., Romascano, David, Villalón-Reina, Julio E., Moreau, Clara A., Almeida Osório, Joana M., Richetin, Sonia, Junod, Vincent, Yu, Paola, Misic, Bratislav, Thompson, Paul M., Fornari, Eleonora, Gygax, Marine Jequier, Jacquemont, Sébastien, Chabane, Nadia, Rodríguez-Herreros, Borja
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	London Nature Publishing Group UK 14.02.2024 Nature Publishing Group
Predmet:	59/57 631/208/2489 631/378 692/699/476/1373 Animals Autism Autism Spectrum Disorder - diagnostic imaging Autism Spectrum Disorder - genetics Behavioral Sciences Biological Psychology Brain - diagnostic imaging Child Child, Preschool Chromosome Deletion Chromosomes, Human, Pair 16 - genetics DNA Copy Number Variations Humans Magnetic Resonance Imaging Medicine Medicine & Public Health Mice Neurosciences Pharmacotherapy Psychiatry White Matter - diagnostic imaging
ISSN:	2158-3188, 2158-3188
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