Associated Papers
WARS2 -Associated Neuropsychiatric Phenotype in Childhood: A Case-Based Review.
Kalita S et al.
Annals of Indian Academy of Neurology, 2025
The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant.
Pauly MG et al.
Genes, 2023
Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy.
Maffezzini C et al.
Molecular Genetics & Genomic Medicine, 2019
Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiency.
Vantroys E et al.
Orphanet Journal of Rare Diseases, 2018
Biallelic mutations in mitochondrial tryptophanyl-tRNA synthetase cause Levodopa-responsive infantile-onset Parkinsonism.
Burke EA et al.
Clinical Genetics, 2018
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability.
Musante L et al.
Human Mutation, 2017
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