Associated Papers
CRISPR activation of the ribosome-associated quality control factor ASCC3 ameliorates fragile X syndrome phenotypes in mice.
Geng J et al.
Science Translational Medicine, 2025
Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3.
Nair D et al.
Hgg Advances, 2021
35047834 (PubMed )
Supplement: mmc1.pdf
Exome sequencing in 51 early onset non-familial CRC cases.
Thutkawkorapin J et al.
Molecular Genetics & Genomic Medicine, 2019
30809968 (PubMed )
Supplement: MGG3-7-e605-s002.xlsx › Supp_Table2__Missense_variants_
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