Article
Integrated DNA methylation analysis reveals a potential role for ANKRD30B in Williams syndrome.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology - 1 Sept 2020
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
Abstract excerpt
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 involves epigenetic modifications; however, the nature of these events remains unclear. To better understand the role...
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