<i>Kmt2c</i>/<i>Mll3</i> Haploinsufficiency Causes Autism-like Behavioral Deficits in Mice

<i>KMT2C</i> (histone lysine N-methyltransferase 2C, also known as <i>MML3</i>, myeloid/lymphoid or mixed-lineage leukemia 3) is a causal gene for Kleefstra syndrome 2, a rare neurodevelopmental disorder. Recent human genetic studies have identified it as a high-risk gene for autism spectrum disorde...

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Bibliografiset tiedot

Päätekijät:	Kaijie Ma, Maria Webb, Haniya Hayder, Luye Qin
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	MDPI AG 2025-11-01
Sarja:	Biomolecules
Aiheet:	autism spectrum disorder <i>KMT2C</i> social behaviors sex cognition
Linkit:	https://www.mdpi.com/2218-273X/15/11/1547
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