Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation

European Journal of Neurology

Volumn 19, Issue 1, 2012, Pages

  Yoon, W T ^a,b   Lee, W Y ^b   Lee, S T ^b   Ahn, J Y ^c   Ki, C S ^b   Cho, J W ^b  

^a School of Medicine   (South Korea)

^b Sungkyunkwan University School of Medicine   (South Korea)

^c Seoul Medical Center   (South Korea)

Author keywords

Foot drop; Hereditary spastic paraplegia; Spastic paraplegia 11 (SPG11) gene; Thin corpus callosum

Indexed keywords

MEMBRANE PROTEIN; PROTEIN SPG11; UNCLASSIFIED DRUG;

ADULT; CASE REPORT; DNA SEQUENCE; ELECTROMYOGRAPHY; GAIT DISORDER; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY SPASTIC PARAPLEGIA WITH THIN CORPUS CALLOSUM; HETEROZYGOSITY; HUMAN; KOREA; LETTER; LIMB WEAKNESS; MALE; MINI MENTAL STATE EXAMINATION; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; RADICULOPATHY; STOP CODON;

CORPUS CALLOSUM; DNA MUTATIONAL ANALYSIS; HUMANS; KOREA; MALE; MUTATION; PROTEINS; SPASTIC PARAPLEGIA, HEREDITARY; YOUNG ADULT;

EID: 84055190685     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2011.03569.x     Document Type: Letter

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