Associated Papers
Genome sequencing of 320 Chinese children with epilepsy: a clinical and molecular study.
Zou D et al.
Brain : a Journal of Neurology, 2021
34145886 (PubMed )
Supplement: awab233_supplementary_data.pdf
Novel Compound Heterozygous Pathogenic Variants in SUOX Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family.
Zhao J et al.
Frontiers in Genetics, 2021
Isolated sulfite oxidase deficiency: a founder mutation.
Mhanni AA et al.
Cold Spring Harbor Molecular Case Studies, 2020
Isolated sulfite oxidase deficiency.
Claerhout H et al.
Journal of Inherited Metabolic Disease, 2018
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