J Korean Neurol Assoc.  2020 Nov;38(4):359-361. 10.17340/jkna.2020.4.27.

SPG11 Mutation in Hereditary Spastic Paraplegia with Thin Corpus Callosum Diagnosed by Targeted Gene Panel Sequencing

Affiliations
  • 1Department of Neurology, Seoul National University Hospital, Seoul, Korea
  • 2Department of Laboratory Medicine, Seoul National University Hospital, Seoul, Korea

Keyword

High-throughput nucleotide sequencing; Hereditary spastic paraplegia; Arnold-Chiari malformation
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