A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation

Journal

  • Journal of human genetics

    Journal of human genetics 60(4), 187-191, 2015-04

    Nature Publishing Group

Codes

  • NII Article ID (NAID)
    40020433141
  • NII NACSIS-CAT ID (NCID)
    AA11206160
  • Text Lang
    ENG
  • ISSN
    1434-5161
  • NDL Article ID
    026332543
  • NDL Call No.
    Z54-H248
  • Data Source
    NDL 
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