Hui Guo
faculty.csu.edu.cn
0000-0002-1570-2545
3 papers found
Refreshing results…
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder
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