De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism
Hiraide, Takuya, Nakashima, Mitsuko, Yamoto, Kaori, Fukuda, Tokiko, Kato, Mitsuhiro, Ikeda, Hiroko, Sugie, Yoko, Aoto, Kazushi, Kaname, Tadashi, Nakabayashi, Kazuhiko, Ogata, Tsutomu, Matsumoto, NaomiLanguage:
english
Journal:
Human Genetics
DOI:
10.1007/s00439-017-1863-y
Date:
January, 2018
File:
PDF, 1.72 MB
english, 2018