Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

Author(s)

Journal

  • Journal of human genetics

    Journal of human genetics 57(5), 338-341, 2012-05-01

    Nature Publishing Group

References:  11

Codes

  • NII Article ID (NAID)
    10030663240
  • NII NACSIS-CAT ID (NCID)
    AA11206160
  • Text Lang
    ENG
  • Article Type
    SHO
  • ISSN
    14345161
  • NDL Article ID
    023661554
  • NDL Call No.
    Z54-H248
  • Data Source
    CJP  NDL 
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