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...

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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379192/
https://www.ncbi.nlm.nih.gov/pubmed/30362171
http://dx.doi.org/10.1111/jcpp.12999

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379192/
https://www.ncbi.nlm.nih.gov/pubmed/30362171
http://dx.doi.org/10.1111/jcpp.12999

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