Biblio
Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies in China Caused by Novel Mutations of PLAA. Clin Genet. 2019.
. HES1 deficiency impairs development of human intestinal mesenchyme by suppressing WNT5A expression. Biochem Biophys Res Commun. 2023;655:50-58.
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