Spectrum of Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 (MCAHS3) Due to Phosphatidylinositol Glycan Biosynthesis Class T (PIGT) Gene Mutations: A Narrative Review
Article in Cureus (May 2024)
The most recent citing publications are shown below. View all 8 publications that cite this research output on Dimensions.
Congenital disorders of glycosylation (CDG): state of the art in 2022
Article in Orphanet Journal of Rare Diseases (October 2023)
Genetic analysis and prenatal diagnosis of a child with Multiple congenital malformations-hypotonia-epilepsy syndrome type3 due to variants of PIGT gene
Article in 中华医学遗传学杂志 (September 2023)