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Valyl-tRNA synthetase 2, mitochondrial
(section)
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==Function== VARS2 gene mutations cause combined oxidative phosphorylation deficiency-20, and are associated with: * early-onset mitochondrial encephalopathies * neurodevelopmental disorder With microcephaly (unusually small skull will be visible at birth) * seizures * cortical atrophy (a wasting in part of the brain matter)<ref name="proteinatlas">{{Cite web|url=https://www.proteinatlas.org/ENSG00000137411-VARS2 | title = VARS2 protein expression summary | last = | first = | author-link =| date = |website=The Human Protein Atlas|archive-url=|archive-date=|url-status=|access-date=2022-01-16}}</ref><ref name="genecards" />
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