Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers
Abstract Deletions and duplications at the 22q11.2 locus are associated with significant neurodevelopmental and psychiatric morbidity. Previous diffusion-weighted magnetic resonance imaging (MRI) studies in 22q11.2 deletion carriers (22q-del) found nonspecific white matter (WM) abnormalities, charac...
Guardado en:
Autores principales: | Johanna Seitz-Holland, Monica Lyons, Leila Kushan, Amy Lin, Julio E. Villalon-Reina, Kang Ik Kevin Cho, Fan Zhang, Tashrif Billah, Sylvain Bouix, Marek Kubicki, Carrie E. Bearden, Ofer Pasternak |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Publishing Group
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/db82ab623713474fa5a3e198e5514566 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME
por: I. A. Tuzankina, et al.
Publicado: (2017) -
Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans
por: PingHsun Hsieh, et al.
Publicado: (2021) -
Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression
por: Amy Lin, et al.
Publicado: (2021) -
22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis
por: Steven de Reuver, et al.
Publicado: (2021) -
Early onset intellectual disability in chromosome 22q11.2 deletion syndrome
por: Cascella,Marco, et al.
Publicado: (2015)