https://www.selleckchem.com/products/U0126.html
Affected individuals present with intellectual disability of varying severity, as well as speech and motor delay, autistic behaviour and additional behavioural manifestations. Our study establishes that de novo coding variants in are involved in a novel monogenic form of NDD, highly similar to the recently reported -related NDD. Our study establishes that de novo coding variants in AGO1 are involved in a novel monogenic form of NDD, highly similar to the recently reported AGO2-related NDD. Recent studies have provided insights into the gu
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