Associated Papers
VARS1 mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domain.
Hiz S et al.
Turkish Journal of Biology = Turk Biyoloji Dergisi, 2022
Biallelic variants in VARS in a family with two siblings with intellectual disability and microcephaly: case report and review of the literature.
Okur V et al.
Cold Spring Harbor Molecular Case Studies, 2018
Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophy.
Stephen J et al.
Human Genetics, 2018
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