Associated Papers
Novel LIAS variants in a patient with epilepsy and profound developmental disabilities.
Wongkittichote P et al.
Molecular Genetics and Metabolism, 2023
Radical S-Adenosylmethionine Enzymes in Human Health and Disease.
Landgraf BJ et al.
Annual Review of Biochemistry, 2016
Novel compound heterozygous LIAS mutations cause glycine encephalopathy.
Tsurusaki Y et al.
Journal of Human Genetics, 2015
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