Integrative network analysis reveals biological pathways associated with Williams syndrome

BACKGROUND: Williams syndrome (WS) is a neurodevelopmental disorder that has been attributed to heterozygous deletions in chromosome 7q11.23 and exhibits a variety of physical, cognitive, and behavioral features. However, the genetic basis of this phenotypic variability is unclear. In this study, we...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:J Child Psychol Psychiatry
Main Authors: Kimura, Ryo, Swarup, Vivek, Tomiwa, Kiyotaka, Gandal, Michael J., Parikshak, Neelroop N., Funabiki, Yasuko, Nakata, Masatoshi, Awaya, Tomonari, Kato, Takeo, Iida, Kei, Okazaki, Shin, Matsushima, Kanae, Kato, Toshihiro, Murai, Toshiya, Heike, Toshio, Geschwind, Daniel H., Hagiwara, Masatoshi
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2018
Assuntos:
Original Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7379192/
https://ncbi.nlm.nih.gov/pubmed/30362171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcpp.12999
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares