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KMID : 0359720200380040359
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Journal of the Korean Neurological Association
2020 Volume.38 No. 4 p.359 ~ p.361
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SPG11 Mutation in Hereditary Spastic Paraplegia with Thin Corpus Callosum Diagnosed by Targeted Gene Panel Sequencing
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Kim Hae-Lim
Min Young-Gi
Hong Sang-Bin
Kim Man-Jin
Seong Moon-Woo
Shin Je-Young
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Abstract
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KEYWORD
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High-throughput nucleotide sequencing, Hereditary spastic paraplegia, Arnold-Chiari malformation
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