Associated Papers
Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome.
Aynekin B et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease, 2026
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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