Associated Papers
Clinical analysis in patients with SPG11 hereditary spastic paraplegia.
Kang YR et al.
Frontiers in Neurology, 2023
Clarification of undiagnosed ataxia using whole-exome sequencing with clinical implications.
Kim M et al.
Parkinsonism & Related Disorders, 2020
Usefulness of comprehensive targeted multigene panel sequencing for neuromuscular disorders in Korean patients.
Park J et al.
Molecular Genetics & Genomic Medicine, 2019
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