Associated Papers
Conserved sequence motifs in human TMTC1, TMTC2, TMTC3, and TMTC4, new O-mannosyltransferases from the GT-C/PMT clan, are rationalized as ligand binding sites.
Eisenhaber B et al.
Biology Direct, 2021
Novel compound variants of the TMTC3 gene cause cobblestone lissencephaly-like syndrome: A case report.
Liu G et al.
Experimental and Therapeutic Medicine, 2020
Endoplasmic reticulum transmembrane protein TMTC3 contributes to O-mannosylation of E-cadherin, cellular adherence, and embryonic gastrulation.
Graham JB et al.
Molecular Biology of the Cell, 2020
A Report on a Family with TMTC3-Related Syndrome and Review.
Hana S et al.
Case Reports in Medicine, 2020
Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly.
Jerber J et al.
American Journal of Human Genetics, 2016
Select a paper to view details