ArticleHuman genetics2018
De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism.
Takuya Hiraide et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
43 papers cite it
this papercites it
ArticleHuman genetics2018
Takuya Hiraide et al.PubMed ↗Publisher ↗
No numbers read from the abstract.