Associated Papers
Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder.
Chen CH et al.
International Journal of Molecular Sciences, 2021
Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.
Doi H et al.
American Journal of Human Genetics, 2011
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