Integrated DNA methylation analysis reveals a potential role for ANKRD30B in Williams syndrome

Williams syndrome (WS) is a rare genetic disorder, caused by a microdeletion at the 7q11.23 region. WS exhibits a wide spectrum of features including hypersociability, which contrasts with social deficits typically associated with autism spectrum disorders. The phenotypic variability in WS likely in...

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Detalles Bibliográficos
Autores principales: Kimura, Ryo, Lardenoije, Roy, Tomiwa, Kiyotaka, Funabiki, Yasuko, Nakata, Masatoshi, Suzuki, Shiho, Awaya, Tomonari, Kato, Takeo, Okazaki, Shin, Murai, Toshiya, Heike, Toshio, Rutten, Bart P. F., Hagiwara, Masatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419304/
https://www.ncbi.nlm.nih.gov/pubmed/32303053
http://dx.doi.org/10.1038/s41386-020-0675-2

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